Month: October 2022

Ethers do have nonbonding electron pairs on their oxygen atoms, 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Electric Literature of 111-90-0.

Shehata, Tamer M.;Elnahas, Hanan M.;Elsewedy, Heba S. research published 《 Development, Characterization and Optimization of the Anti-Inflammatory Influence of Meloxicam Loaded into a Eucalyptus Oil-Based Nanoemulgel》, the research content is summarized as follows. The purpose of the present study was to explore the influence of a certain natural essential oil, namely eucalyptus oil, as an anti-inflammatory agent in addition to its prospective role in enhancing the action of meloxicam in reducing inflammation. As far as we know, this has been the first integration of meloxicam and eucalyptus essential oil into a nanoemulgel formulation intended for topical use. Primarily, eucalyptus oil was utilized in developing a nanoemulsion formulation incorporating meloxicam. A 22 factorial design was constructed using two independent variables (oil concentration and surfactant concentration) with two responses (particle size and % of in vitro release). One optimized formula was selected depending on the desirability function and subjected to a stability study. The optimized nanoemulsion was mixed with HPMC as a gelling agent to produce a meloxicam-loaded nanoemulgel, which was examined for its properties, stability, in vitro release and ex vivo permeation. Eventually, the anti-inflammatory activity was evaluated and compared with a placebo and corresponding gel formulation. The developed nanoemulgel revealed acceptable phys. characteristics to be applied topically. Studying of the in vitro release was conducted successfully for 6 h. The ex vivo permeation from the nanoemulgel formulations was prompted, showing an appropriate value of the steady-state transdermal flux (SSTF). As a final point, the anti-inflammatory activity of the developed nanoemulgel revealed a valued anti-inflammatory influence. Addnl., the concurrence of eucalyptus essential oil and meloxicam was assured, and their potential in combating and lowering inflammation was supported.

Electric Literature of 111-90-0, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers do have nonbonding electron pairs on their oxygen atoms, 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Recommanded Product: Diethylene Glycol Monoethyl Ether.

Sharma, Shubham;Sharma, Samriti;Singh, Manjeet;Singh, Jeetinder;Sharma, Meena research published 《 Density, Speed of Sound, and Viscosity for Binary Liquid Mixtures of 2-(2-Ethoxyethoxy)ethanol with Methyl Acrylate, Ethyl Acrylate, or Butyl Acrylate from T = 288.15 to 318.15 K and P = 101 kPa》, the research content is summarized as follows. In this study, the d. (ρ), speed of sound (u), and viscosity (η) of the binary liquid mixtures of an industrially important solvent 2-(2-ethoxyethoxy)ethanol (carbitol) with acrylic esters [methyl acrylate, Et acrylate, and Bu acrylate (BA)] have been measured over the entire composition range at temperatures from T = 288.15 to 318.15 K and at atm. pressure P = 101 kPa. The excess molar volume (V_m^E), excess isentropic compressibility (κ_s^E), and viscosity deviations (Δη) have been calculated from the related exptl. data. All excess properties are neg. at all temperatures for all the mixtures, suggesting the compactness of binary mixture except the pos. V_m^E values for some concentrations of BA mixtures Deviation from ideality increases with rising temperature for both excess molar volume and excess isentropic compressibility but a decrease in deviation from ideality with temperature rise has been observed for viscosity deviations. Finally, excess properties have been fitted to the Redlich-Kister polynomial.

111-90-0, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., Recommanded Product: Diethylene Glycol Monoethyl Ether

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers can again be classified into two varieties: if the alkyl or aryl groups are the same on both sides of the oxygen atom, 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. Then it is a simple or symmetrical ether, whereas if they are different, the ethers are called mixed or unsymmetrical ethers. Formula: C6H14O3.

Sharma, Monika;Kaur, Jaswinder;Rakshe, Siddhi;Sharma, Nishant;Khunt, Dignesh;Khairnar, Amit research published 《 Intranasal Exposure to Low-Dose Rotenone Induced Alpha-Synuclein Accumulation and Parkinson′s Like Symptoms Without Loss of Dopaminergic Neurons》, the research content is summarized as follows. Epidemiol. Parkinson′s disease (PD) is associated with chronic ingestion or inhalation of environmental toxins leading to the development of motor symptoms. Though neurotoxin-based animal models played a major role in understanding diverse pathogenesis, they failed to identify the risk assessment due to uncommon route of toxin exposure. Toward this, the available neurotoxin-based intranasal (i.n.) PD models targeting olfactory bulb (OB) have demonstrated the dopaminergic (DAergic) neurodegeneration in both OB and substantia nigra (SN). Despite that, the studies detecting the alpha-synuclein (α-syn) accumulation in OB and its progression to other brain regions due to inhalation of environmental toxins are still lacking. Herein, we developed oil in water microemulsion of rotenone administered intranasally to the mice at a dose which is not detectable in blood, brain, and olfactory bulb by LCMS method. Our data reveals that 9 wk of rotenone exposure did not induce olfactory and motor dysfunction. Conversely, after 16 wk of washout period, rotenone treated mice showed both olfactory and motor impairment, along with α-syn accumulation in the OB and striatum without glial cell activation and loss of dopaminergic neurons. The results depict the progressive nature of the developed model and highlight the role of α-syn in PD like pathol. or symptoms. Together, our findings suggest the adverse consequences of early exposure to the environmental toxins on the olfactory system for a shorter period with relevance to the development of synucleinopathy or Parkinson′s disease in its later stage.

Formula: C6H14O3, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 38256-93-8, formula is C4H11NO, Name is 2-Methoxy-N-methylethanamine.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Recommanded Product: 2-Methoxy-N-methylethanamine.

Shao, Min;Chen, Xiaojuan;Yang, Fang;Song, Xiaojuan;Zhou, Yang;Lin, Qianmeng;Fu, Ying;Ortega, Raquel;Lin, Xiaojing;Tu, Zhengchao;Patterson, Adam V.;Smaill, Jeff B.;Chen, Yongheng;Lu, Xiaoyun research published 《 Design, Synthesis, and Biological Evaluation of Aminoindazole Derivatives as Highly Selective Covalent Inhibitors of Wild-Type and Gatekeeper Mutant FGFR4》, the research content is summarized as follows. A series of aminoindazole derivatives I [R¹ = 1-(2,6-dichloro-3-fluoro-phenyl)ethyl, 1-(2,6-dichlorophenyl)ethyl, (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, (3,5-dichloro-4-pyridyl)methyl, 1-(3,5-dichloro-4-pyridyl)propyl; R² = H, Me, Cl, etc.; R³ = H, MeO; R⁴ = H, 4-methylpiperazin-1-yl, morpholino, etc.] was designed and synthesized as new irreversible inhibitors of wild-type and gatekeeper mutant FGFR4. One representative compound I [R¹ = (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, R² = F, R³ = H, R⁴ = 4-morpholino-1-piperidyl] exhibited excellent potency against FGFR4, FGFR4^V550L and FGFR4^V550M with nanomolar activity in both the biochem. and cellular assays while sparing FGFR1/2/3. While compound I [R¹ = (1R)-1-(3,5-dichloro-4-pyridyl)ethyl, R² = F, R³ = H, R⁴ = 4-morpholino-1-piperidyl] demonstrated modest in vivo antitumor efficacy in nude mice bearing the Huh-7 xenograft model consistent with its unfavorable pharmacokinetic properties, it provided a promising new starting point for future drug discovery combating FGFR4 gatekeeper mediated resistance in HCC patients.

Recommanded Product: 2-Methoxy-N-methylethanamine, 2-Methoxy-N-methylethanamine is a useful research compound. Its molecular formula is C4H11NO and its molecular weight is 89.14 g/mol. The purity is usually 95%.
2-Methoxy-N-methylethanamine is a drug that binds to the cannabinoid receptor CB1. It has been shown to be effective in the treatment of cardiac arrhythmia and may also be used as an anti-inflammatory drug. 2MEMEA has been shown to have pharmacokinetic properties that are different from those of other amines, which may be due to its ability to form hydrogen bonds with water molecules. 2MEMEA also has diversified effects on some types of cancer cells, including hyperproliferative and amine-dependent cancers., 38256-93-8.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Category: ethers-buliding-blocks.

Shamsi, Ali;Hashemian, Saeedeh research published 《 Structural, magnetic and adsorptive properties of nano spinel of cobalt aluminate doped with nickel for Cr(VI) removal》, the research content is summarized as follows. Nanocrystallines of cobalt aluminate spinel doped with Nickel (MAl₂O₄; M = Co²⁺, Ni²⁺) were synthesized by sol-gel method. The MAl2O4 samples were prepared by using aluminum nitrate; cobalt nitrate, nickel nitrate, citric acid and diethylene glycol mono Et ether as precursor materials. The nanocrystallines spinel were characterized by Fourier transform IR spectroscopy (FTIR), X-ray diffraction(XRD), Thermal gravimetric (TGA), Scanning electron microcopy (SEM) with the energy dispersive X-ray spectroscopy (EDX) methods. The Sp. surface area of the synthesized powders was measured with a Brunauer-Emmet-Teller (BET) apparatus using N₂ adsorption. According to obtained XRD patterns the formation of single phase MAl₂O₄ completed up 800 °C. The average crystallite′s sizes spinel and sp. surface area at 800 °C were estimated about 11.07 nm and 154 m² g^-1, resp. The results of SEM anal. show that the nanoparticles shape are as spherical shape, uniform and a little agglomerated. The magnetic behavior of spinels showed the magnetization decreased with increasing nickel ions. Adsorption of Cr(VI) by as prepared spinels were considered. The highest percent of Cr(VI) adsorption was occurred at contact time of 45 min, pH 7.0, and adsorbent dose of 2 g L^-1. The order of adsorption capacity of sorbent samples for Cr(VI) removal was as follow: Ni_0.5Cu_0.5Al₂O₄ >Ni_0.7Cu_0.3Al₂O₄ >Ni0.3Cu0.7Al₂O₄>NiAl₂O₄> CoAl₂O₄. Kinetic studies indicated that the adsorption process follows by pseudo second-order model. Thermodn. results revealed that the adsorption of Cr(VI) is endothermic, spontaneously process and feasible in the range of 298-338 K.

Category: ethers-buliding-blocks, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers are a class of organic compounds that contain an ether group—an oxygen atom connected to two alkyl or aryl groups. 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether.They have the general formula R–O–R′, where R and R′ represent the alkyl or aryl groups. Reference of 111-90-0.

Shakeel, Faiyaz;Alshehri, Sultan;Ghoneim, Mohammed M.;Martinez, Fleming;Pena, Maria.;Jouyban, Abolghasem;Acree, William E. research published 《 Solubility of tadalafil in aqueous mixtures of Transcutol and PEG 400 revisited: correlation, thermodynamics and preferential solvation》, the research content is summarized as follows. Mole fraction solubilities of tadalafil (3) in aqueous mixtures of Transcutol and PEG 400 at temperatures from 298.15 to 333.15 K were analyzed following Hildebrand solubility parameters. Cosolvency models for representing tadalafil solubility at various temperatures were also provided for correlation/prediction purposes. Apparent thermodn. quantities for tadalafil dissolution processes were calculated based on van′t Hoff and Gibbs equations. Non-linear enthalpy-entropy compensation was observed for tadalafil transfer from more polar to less polar solvent systems. Preferential solvation parameters of tadalafil at 298.15 and 313.15 K were determined by means of the inverse Kirkwood-Buff integrals (IKBI). Tadalafil is preferentially solvated by water in water-rich mixtures of Transcutol but preferentially solvated by Transcutol in mixtures of 0.12 < x1 < 1.00. In the former case, this result could be due to hydrophobic hydration around the non-polar moieties of tadalafil. Otherwise, tadalafil is preferentially solvated by PEG 400 in all the aqueous mixtures

Reference of 111-90-0, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers feature bent C–O–C linkages. In dimethyl ether, the bond angle is 111° and C–O distances are 141 pm. 73724-45-5, formula is C18H17NO5, Name is Fmoc-Ser-OH. The barrier to rotation about the C–O bonds is low. The bonding of oxygen in ethers, alcohols, and water is similar. In the language of valence bond theory, the hybridization at oxygen is sp3. Formula: C18H17NO5.

Sgorbati, Clara;Lo Presti, Eliana;Bergamaschi, Greta;Sani, Monica;Volonterio, Alessandro research published 《 Solid-phase synthesis of Gly-Ψ[CH(CF₃)NH]-peptides》, the research content is summarized as follows. The solid-phase synthesis of Gly-Ψ[CH(CF₃)NH]-peptides is presented. In order to achieve this goal, the synthesis of Gly-Ψ[CH(CF₃)NH]-dipeptides having the C-terminus unprotected, the N-terminus protected as Fmoc- or Teoc-, and possibly side chain functionalities protected with acid-labile protecting groups has been developed. A selected small library of six peptidomimetics, encompassing analogs of biol. relevant peptides, have been obtained in high purity.

73724-45-5, Fmoc-Ser-OH, also known as Fmoc-Ser-OH, is a useful research compound. Its molecular formula is C18H17NO5 and its molecular weight is 327.3 g/mol. The purity is usually 95%.
Fmoc-L-Ser-OH is a synthetic peptide that belongs to the group of glycopeptides. It is used as a model for such compounds and has been shown to have antimicrobial activity in vitro against gram-positive bacteria, especially Staphylococcus epidermidis. This compound was synthesized from 3-mercaptopropionic acid and chloride in the presence of hydroxyl groups and epidermal growth factor. The synthetic pathway can be divided into three steps: (1) condensation of 3-mercaptopropionic acid with hydrochloric acid to yield 3-mercaptoacrylic acid; (2) esterification of 3-mercaptoacrylic acid with glycine to form Fmoc-L-Ser; and (3) deprotection of Fmoc protecting group., Formula: C18H17NO5

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Formula: C8H11BO4.

Serrano, Jose Luis;Gaware, Sujeet;Perez, Jose Antonio;Perez, Jose;Lozano, Pedro;Kori, Santosh;Dandela, Rambabu;Sanghvi, Yogesh S.;Kapdi, Anant R. research published 《 Quadrol-Pd(II) complexes: phosphine-free precatalysts for the room-temperature Suzuki-Miyaura synthesis of nucleoside analogues in aqueous media》, the research content is summarized as follows. Com. available Quadrol, N,N,N′,N′-tetrakis(2-hydroxypropyl)ethylenediamine (THPEN), has been used for the first time as a NN-donor neutral hydrophilic ligand in the synthesis and characterization of new water soluble palladium(II) complexes containing chloride, phthalimidate or saccharinate as co-ligands. [PdCl₂(THPEN)] (1) [Pd(phthal)2(THPEN)] (2), [Pd(sacc)₂(THPEN)] (3) and the analogous complex with the closely related N,N,N′,N′-tetrakis(2-hydroxyethyl)ethylenediamine (THEEN) [Pd(sacc)₂(THEEN)] (4) were efficiently prepared in a one-pot reaction from [PdCl₂(CH₃CN)₂] or Pd(OAc)₂. Structural characterization of 1 and 3 by single crystal X-ray diffraction produced the first structures reported to date of palladium complexes with Quadrol. The resultant palladium complexes are highly soluble in water and were found to be effective as phosphine-free catalysts for the synthesis of functionalized nucleoside analogs under room-temperature Suzuki-Miyaura cross-coupling conditions between 5-iodo-2′-deoxyuridine (& 5-iodo-2′-deoxycytidine) with different aryl boronic acids in neat water. This is the first report of the coupling process performed on nucleosides in water at room temperature

Formula: C8H11BO4, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., 122775-35-3.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers do have nonbonding electron pairs on their oxygen atoms, 111-90-0, formula is C6H14O3, Name is Diethylene Glycol Monoethyl Ether. The ability to form hydrogen bonds with other compounds makes ethers particularly good solvents for a wide variety of organic compounds and a surprisingly large number of inorganic compounds. Name: Diethylene Glycol Monoethyl Ether.

Schmied, Fabian-Pascal;Bernhardt, Alexander;Engel, Andrea;Klein, Sandra research published 《 A Customized Screening Tool Approach for the Development of a Self-Nanoemulsifying Drug Delivery System (SNEDDS)》, the research content is summarized as follows. The present study focused on establishing a novel, (pre-)screening approach that enables the development of promising performing self-nanoemulsifying drug delivery systems (SNEDDSs) with a limited number of experiments The strategic approach was based on first identifying appropriate excipients (oils/lipids, surfactants, and co-solvents) providing a high saturation solubility for lipophilic model compounds with poor aqueous solubility Excipients meeting these requirements were selected for SNEDDS development, and a special triangular mixture design was applied for determining excipient ratios for the SNEDDS formulations. Celecoxib and fenofibrate were used as model drugs. Formulations were studied applying a specific combination of in vitro characterization methods. Specifications for a promising SNEDDS formulation were self-imposed: a very small droplet size (< 50 nm), a narrow size distribution of these droplets (PDI < 0.15) and a high transmittance following SNEDDS dispersion in water (> 99% in comparison with purified water). Excipients that provided a nanoemulsion after dispersion were combined, and ratios were optimized using a customized mapping method in a triangular mixture design. The best performing formulations were finally studied for their in vitro release performance. Results of the study demonstrate the efficiency of the customized screening tool approach. Since it enables successful SNEDDS development in a short time with manageable resources, this novel screening tool approach could play an important role in future SNEDDS development.

Name: Diethylene Glycol Monoethyl Ether, Diethylene glycol monoethyl ether appears as a colorless, slightly viscous liquid with a mild pleasant odor. Flash point near 190°F. Used to make soaps, dyes, and other chemicals.
Diethylene glycol monoethyl ether is a primary alcohol that is ethanol substituted by a 2-ethoxyethoxy group at position 2. It has a role as a protic solvent. It is a diether, a primary alcohol and a hydroxypolyether. It derives from a diethylene glycol., 111-90-0.

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem

Ethers lack the hydroxyl groups of alcohols. Without the strongly polarized O―H bond, ether molecules cannot engage in hydrogen bonding with each other. 122775-35-3, formula is C8H11BO4, Name is 3,4-Dimethoxyphenylboronic acid. Ethers do have nonbonding electron pairs on their oxygen atoms, however, and they can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O―H or N―H bonds. Formula: C8H11BO4.

Schmidt, Tanno A.;Sparr, Christof research published 《 Catalyst-Controlled Stereoselective Barton-Kellogg Olefination》, the research content is summarized as follows. Herein, the direct catalyst control is achieved by a stereoselective Barton-Kellogg olefination with enantio- and diastereocontrol for various bistricyclic aromatic enes I (R = H, F, Br, 2,6-dimethoxyphenyl; R¹ = H, Me, Ph, 3,5-dichlorophenyl, etc.) was reported. Using Rh₂(S-PTAD)₄ as catalyst, several diazo compounds II were selectively coupled with a thioketone to give one of the four anti-folded overcrowded alkene stereoisomers I upon reduction Complete stereodivergence was reached by catalyst control in combination with distinct thiirane reductions to provide all four stereoisomers I (R = H, R¹ = 3,5-dimethoxyphenyl) with e.r. values of up to 99:1. This strategy will enable the synthesis of topol. unique overcrowded alkenes I for functional materials, catalysis, energy- and electron transfer, and bioactive compounds

122775-35-3, 3,4-Dimethoxyphenylboronic acid is a useful research compound. Its molecular formula is C8H11BO4 and its molecular weight is 181.98 g/mol. The purity is usually 95%.
3,4-Dimethoxyphenylboronic acid contains varying amounts of anhydride.
3,4-Dimethoxyphenylboronic acid is a bacterial mutagen. A useful intermediate for organic synthesis.
3,4-Dimethoxyphenylboronic acid is a boronate ester that has been shown to be an effective coupling partner for the Suzuki reaction. It has also been used in cancer therapy and as a photochemical probe for the study of biological properties. 3,4-Dimethoxyphenylboronic acid has been shown to demethylate DNA and inhibit methionine aminopeptidase activity. It also cross-couples with halides, such as chlorides or iodides, and activates tertiary alcohols. 3,4-Dimethoxyphenylboronic acid is soluble in organic solvents and can be used in supramolecular chemistry., Formula: C8H11BO4

Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem