Laguerre, Aurelien’s team published research in Journal of the American Chemical Society in 2019 | CAS: 4637-24-5

N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5) belongs to anime. Amines can be classified according to the nature and number of substituents on nitrogen. Aliphatic amines contain only H and alkyl substituents. Aromatic amines have the nitrogen atom connected to an aromatic ring.Important amines include amino acids, biogenic amines, trimethylamine, and aniline. Inorganic derivatives of ammonia are also called amines, such as monochloramine (NClH2).COA of Formula: C5H13NO2

In 2019,Journal of the American Chemical Society included an article by Laguerre, Aurelien; Hauke, Sebastian; Qiu, Jian; Kelly, Martin J.; Schultz, Carsten. COA of Formula: C5H13NO2. The article was titled 《Photorelease of 2-Arachidonoylglycerol in Live Cells》. The information in the text is summarized as follows:

2-Arachidonoylglycerol (2-AG) is acting as a full agonist of cannabinoid receptor 1 and 2. Direct manipulation of 2-AG levels is a challenging task. The amphiphilic properties and the instability of 2-AG in aqueous media complicate its use as a drug-like mol. Addnl., inhibition of the protein machinery that regulates 2-AG levels may also affect other monoacylglycerols. Therefore, we developed a novel method to elevate 2-AG levels with a flash of light. The resulting tool is a photoactivatable “”caged”” 2-arachidonoylglycerol (cg2-AG) allowing for the rapid photorelease of the signaling lipid in live cells. We characterized the mechanism of uncaging and the effect of 2-AG on the regulation of the β-cell signaling network. After uncaging of 2-AG, we monitored calcium levels, CB1-GIRK channel coupling, and CB1-mediated inhibition of adenylate cyclase and protein kinase A activity. In the experiment, the researchers used N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5COA of Formula: C5H13NO2)

N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5) belongs to anime. Amines can be classified according to the nature and number of substituents on nitrogen. Aliphatic amines contain only H and alkyl substituents. Aromatic amines have the nitrogen atom connected to an aromatic ring.Important amines include amino acids, biogenic amines, trimethylamine, and aniline. Inorganic derivatives of ammonia are also called amines, such as monochloramine (NClH2).COA of Formula: C5H13NO2

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

Karimi-Chayjani, Reyhaneh’s team published research in Research on Chemical Intermediates in 2019 | CAS: 135-02-4

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.Electric Literature of C8H8O2

The author of 《New magnetic nanocatalyst containing a bis-dicationic ionic liquid framework for Knoevenagel condensation reaction》 were Karimi-Chayjani, Reyhaneh; Daneshvar, Nader; Shirini, Farhad; Tajik, Hassan. And the article was published in Research on Chemical Intermediates in 2019. Electric Literature of C8H8O2 The author mentioned the following in the article:

Bis[(3-aminopropyl)triethoxysilane]dichloride immobilized on magnetic nano-γ-Fe2O3@SiO2 were prepared After characterization, the reagent was used for efficient promotion of the Knoevenagel reaction, achieving high reaction rates and yields. Also, the recovery and reusability of the catalyst were excellent for the studied reaction. In the experiment, the researchers used 2-Methoxybenzaldehyde(cas: 135-02-4Electric Literature of C8H8O2)

2-Methoxybenzaldehyde(cas: 135-02-4) is used as a flavor agent in foods including nonalcoholic/alcoholic beverages, baked goods, chewing gum, confections, frozen dairy, fruit ices, hard/soft candy, instant coffee, tea, Jams, jellies, and milk products. It also has been used to obtain good enantioselectivities using Cu(OAc)(2)-bis(oxazolines) via hydrogen bonding in asymmetric Henry reaction.Electric Literature of C8H8O2

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

Wang, Pengfei’s team published research in Frontiers in Chemistry (Lausanne, Switzerland) in 2020 | CAS: 673-22-3

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Recommanded Product: 673-22-3

《””Turn-on”” fluorescent biosensors for high selective and sensitive detection of Al3+ ion》 was written by Wang, Pengfei; Liu, Lijie; Meng, Fanda; Khan, Maroof Ahmad; Li, Hui. Recommanded Product: 673-22-3 And the article was included in Frontiers in Chemistry (Lausanne, Switzerland) in 2020. The article conveys some information:

A series of new compounds (1-4) based on pyrrole hydrazone Schiff bases were designed and synthesized. The interactions of these new compounds with metal ions and their fluorescent recognition were investigated. All compounds showed “”turn-on”” fluorescence in the presence of Al3+ in aqueous solution Their sensing behaviors with Al3+ were studied using photophys. experiments, ESI-MS spectrometry anal., 1H NMR titration, and DFT calculation The detection limits of 1-4 for the anal. of Al3+ were found to reach a 10-8 M level in aqueous solution, which are far lower than the WHO guidelines for drinking water (7.41 mM for Al3+). A high selectivity test paper has been fabricated for Al3+ detection based on sensor 3. Theor. calculations (DFT) have been carried out to elucidate the configuration of 1-4 and their Al complexes and rationalize exptl. absorption data. In the experiment, the researchers used 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Recommanded Product: 673-22-3)

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is employed in the synthesis of Schiff base ligand. It is applied as a reactant in the synthesis of LPA1R antagonists used in the inhibition of LPA-induced proliferation and contraction of normal human lung fibroblasts. Also used in the synthesis of tyrosine kinase 6 proteinase inhibitors.Recommanded Product: 673-22-3

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

Durgadevi, Ravindran’s team published research in Colloids and Surfaces, B: Biointerfaces in 2020 | CAS: 673-22-3

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is the main component of root bark essential oil of Periploca sepium Bunge. It is a potential tyrosinase inhibitor present in African medicinal plants. 2-Hydroxy-4-methoxybenzaldehyde was used in the synthesis of Schiff base ligand.Product Details of 673-22-3

《Attenuation of Proteus mirabilis colonization and swarming motility on indwelling urinary catheter by antibiofilm impregnation: An in vitro study》 was written by Durgadevi, Ravindran; Kaleeshwari, Ramaiah; Swetha, Thirukannamangai Krishnan; Alexpandi, Rajaiah; Karutha Pandian, Shunmugaiah; Veera Ravi, Arumugam. Product Details of 673-22-3 And the article was included in Colloids and Surfaces, B: Biointerfaces in 2020. The article conveys some information:

Proteus mirabilis is one of the important etiol. agents of urinary tract infections (UTI), which complicates the long-term urinary catheterization process in clin. settings. Owing to its crystalline biofilm forming ability and flagellar motility, elimination of P. mirabilis from urinary system becomes very difficult. Thus, the present study is focused to prepare antibiofilm-impregnated Silicone Foley Catheter (SFC) to prevent P. mirabilis instigated UTIs. Through solvent swelling method, the antibiofilm compounds such as linalool (LIN) and 2-hydroxy-4-methoxy benzaldehyde (HMB) were successfully infused into SFCs. Surface topog. was studied using AFM anal., which unveiled the unmodified surface roughness of normal and antibiofilm-impregnated SFCs. In addition, UV-spectrometric and FT-IR analyses revealed good impregnation efficacy and prolonged stability of antibiofilm compounds Further, in vitro biofilm biomass quantification assay exhibited a maximum of 87% and 84% crystalline biofilm inhibition in LIN (350μg/cm3) and HMB (120μg/cm3) impregnated SFCs, resp. against P. mirabilis in artificial urine medium. Also, the LIN & HMB-impregnated SFCs demonstrated long-term crystalline biofilm inhibitory activity for more than 30 days, which is ascribed to the sustained release of the compounds Furthermore, the results of swarming motility anal. revealed the efficacy of antibiofilm-impregnated catheters to mitigate the migration of pathogens over them. Thus, antibiofilm-impregnated catheter is proposed to act as a suitable strategy for reducing P. mirabilis infections and associated complications in longterm urinary catheter users. The results came from multiple reactions, including the reaction of 2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Product Details of 673-22-3)

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is the main component of root bark essential oil of Periploca sepium Bunge. It is a potential tyrosinase inhibitor present in African medicinal plants. 2-Hydroxy-4-methoxybenzaldehyde was used in the synthesis of Schiff base ligand.Product Details of 673-22-3

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

El-Attar, Rehab O.’s team published research in Journal of the Iranian Chemical Society in 2020 | CAS: 33100-27-5

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Application of 33100-27-5

《Potentiometric screen-printed sensor for determination of oxybutynin hydrochloride》 was written by El-Attar, Rehab O.; Hendawy, Hassan A. M.; Khaled, Elmorsy. Application of 33100-27-5 And the article was included in Journal of the Iranian Chemical Society in 2020. The article conveys some information:

Abstract: The present work describes the fabrication of disposable screen-printed oxybutynin hydrochloride (OXB) potentiometric sensors. The electrode matrix composition was investigated on the basis of the effect of the nature and concentration of sensing ionophores, anionic sites, plasticizers and nanomaterials. Incorporation of single-walled carbon nanotubes (SWCNTs) as transducer and (2, 3, 6-tri-O-methyl)-β-cyclodextrin as mol. recognition elements in the electrode matrix improved both the sensitivity and selectivity of the sensor towards oxybutynin hydrochloride. The fabricated sensors showed Nernstian slope of 57.5 ± 1.0 mV decade-1 in the concentration range from 10-6 to 10-2 mol L-1 OXB with detection limit of 8 x 10-7 mol L-1. Moreover, the presence of SWCNTs in the electrode matrix enhanced the potential reading stability, response time (< 4 s) and increased life time of the sensors (5 mo). The developed sensors were successfully applied for determination of OXB in pharmaceutical formulations and biol. fluids with agreeable average recoveries compared with the official methods. The experimental part of the paper was very detailed, including the reaction process of 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Application of 33100-27-5)

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Application of 33100-27-5

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

Shalimov, Oleksandr’s team published research in ARKIVOC (Gainesville, FL, United States) in 2022 | CAS: 150-19-6

m-Methoxyphenol(cas: 150-19-6) may be used in synthesis of:C(4) symmetric calix[4]resorcinarene, 2-nitroso-5-methoxyphenol, 6-methoxy-2(3H)-benzoxazoloneRelated Products of 150-19-6

In 2022,Shalimov, Oleksandr; Rusanov, Eduard; Onys’ko, Petro published an article in ARKIVOC (Gainesville, FL, United States). The title of the article was 《Novel convenient approach to 1,4,2-benzodithiazine-1,1-dioxides and 1,2,3-benzoxathiazine-2,2-dioxides》.Related Products of 150-19-6 The author mentioned the following in the article:

A new effective method for the construction of 1,4,2-benzodithiazine I (R = H, Cl); R1 = H, OMe; R2 = H, Cl, Me; R3 = H, Me, OMe; R2 R3 = -CH=CH-CH=CH-; and 1,2,3-benzoxathiazine II (R4 = H, OH, OMe; R5 = H, OMe) scaffolds, based on the use of easily accessible N-chlorosulfonyltrichloroacetimidoyl chloride, has been developed. Reactions of thiophenols 2-R-3-R1-4-R2-5-R3C6H1SH involved an initial nucleophilic substitution at the imine carbon atom with a thiol sulfur atom, followed by intramol. sulfonylation of the benzene ring. Phenols 3-R4-5-R5-C6H3OH exhibit opposite regioselectivity and react by electrophilic imidoylation of the ortho-carbon atom of the benzene ring (C-C bond formation) and sulfonation of the phenol oxygen atom. Synthesized 1,4,2-benzodithiazine-1,1-dioxides Iexhibit growth-stimulating activity on monocotyledonous winter wheat ”Bezosta” and dicotyledonous plants Barbarea arcuate. In addition to this study using m-Methoxyphenol, there are many other studies that have used m-Methoxyphenol(cas: 150-19-6Related Products of 150-19-6) was used in this study.

m-Methoxyphenol(cas: 150-19-6) may be used in synthesis of:C(4) symmetric calix[4]resorcinarene, 2-nitroso-5-methoxyphenol, 6-methoxy-2(3H)-benzoxazoloneRelated Products of 150-19-6

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

Durrant, James P.’s team published research in Angewandte Chemie, International Edition in 2022 | CAS: 33100-27-5

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Product Details of 33100-27-5

In 2022,Durrant, James P.; Day, Benjamin M.; Tang, Jinkui; Mansikkamaki, Akseli; Layfield, Richard A. published an article in Angewandte Chemie, International Edition. The title of the article was 《Dominance of Cyclobutadienyl Over Cyclopentadienyl in the Crystal Field Splitting in Dysprosium Single-Molecule Magnets》.Product Details of 33100-27-5 The author mentioned the following in the article:

Replacing a monoanionic cyclopentadienyl (Cp) ligand in Dy single-mol. magnets (SMMs) with a dianionic cyclobutadienyl (Cb) ligand in the sandwich complexes [(η4-Cb””)Dy(η5-C5Me4tBu)(BH4)]- (1), [(η4-Cb””)Dy(η8-Pn )K(THF)] (2) and [(η4-Cb””)Dy(η8-Pn )]- (3) leads to larger energy barriers to magnetization reversal (Cb”” = C4(SiMe3)4, Pn = 1,4-di(tri-isopropylsilyl)pentalenyl). Short distances to the Cb”” ligands and longer distances to the Cp ligands in 1-3 are consistent with the crystal field splitting being dominated by the former. Theor. anal. shows that the magnetic axes in the ground Kramers doublets of 1-3 are oriented towards the Cb”” ligands. The theor. axiality parameter and the relative axiality parameter Z and Zrel are introduced to facilitate comparisons of the SMM performance of 1-3 with a benchmark SMM. Increases in Z and Zrel when Cb”’ replaces Cp signposts a route to SMMs with properties that could surpass leading systems. In the experiment, the researchers used 1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5Product Details of 33100-27-5)

1,4,7,10,13-Pentaoxacyclopentadecane(cas: 33100-27-5) is a member of crown ether Ligands. Crown-ethers are macrocyclic polyethers capable of forming host-guest complexes, especially with inorganic and organic cations. Crown-ethers can incorporate protonated primary amine compounds by formation of ion-dipole bonds with the oxygen atoms of the chiral selector. Crown-ethers have been widely used for the separation of several pharmaceuticals both in aqueous and non-aqueous media. Product Details of 33100-27-5

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

Abad, Nadeem’s team published research in Journal of Biomolecular Structure and Dynamics in 2022 | CAS: 4637-24-5

N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Application of 4637-24-5

Application of 4637-24-5In 2022 ,《Insights into the crystal structure of two newly synthesized quinoxalines derivatives as potent inhibitor for c-Jun N-terminal kinases》 appeared in Journal of Biomolecular Structure and Dynamics. The author of the article were Abad, Nadeem; El Bakri, Youness; Lai, Chin-Hung; Karthikeyan, Subramani; Ramli, Youssef; Ferfra, Souad; Mague, Joel T.; Essassi, El Mokhtar. The article conveys some information:

Two new compounds namely, Et (2E)-3-(dimethylamino)-2-(3-methoxyquinoxalin-2-yl)propen-2-enoate () and Et 2-(3-oxo-4-(prop-2-yn-1-yl)-3,4-dihydroquinoxalin-2-yl)-3-phenylpropanoate () have been synthesized from Et 2-(oxo-3,4-dihydroquinoxalin-2-yl) acetate (). The compounds were characterized using NMR (1H and 13C), Fourier transform IR and confirmed by single crystal X-ray diffraction studies. The quinoxaline portion of is almost planar with the substituent containing the dimethylamino and carboxyethyl groups rotated well out of its mean plane. In the crystal, C-H···O and C-H···N hydrogen bonds as well as C-H···Π(ring) interactions form chains having a U-shaped cross-section and running along the c-axis direction. Two sets of pair-wise C-H···O hydrogen bonds connect the chains into corrugated sheets. In, the three substituents on the dihydroquinoxaline moiety are rotated well out of its mean plane. Three sets of C-H···O hydrogen bonds as well as C-H···π(ring) and π-π-stacking interactions form layers approx. parallel to [001]. These are associated along the c-axis direction by addnl. C-H···π(ring) interactions. Addnl., the Hirshfeld surface analyses showed that the H···H contact is the most important interaction for both and In addition to this, mol. docking and dynamics studies were carried for these two compounds with the c-Jun N-terminal kinases (JNK1) mol.Communicated by Ramaswamy H. The experimental part of the paper was very detailed, including the reaction process of N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5Application of 4637-24-5)

N,N-Dimethylformamide Dimethyl Acetal(cas: 4637-24-5) belongs to anime. Acylation is one of the most important reactions of primary and secondary amines; a hydrogen atom is replaced by an acyl group (a group derived from an acid, such as RCOOH or RSO3H, by removal of ―OH, such as RC(=O)―, RS(O)2―, and so on). Reagents may be acid chlorides (RCOC1, RSO2C1), anhydrides ((RCO)2O), or even esters (RCOOR′); the products are amides of the corresponding acids.Application of 4637-24-5

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

Buonsenso, Fabio’s team published research in International Journal of Molecular Sciences in 2021 | CAS: 150-19-6

m-Methoxyphenol(cas: 150-19-6) may be used as an analytical standard for the determination of the analyte in wine, coffee beans, wood samples, and mainstream smoke by gas chromatography (GC) based techniques.Application of 150-19-6

Application of 150-19-6In 2021 ,《Exploring the Assembly of Resorc[4]arenes for the Construction of Supramolecular Nano-Aggregates》 appeared in International Journal of Molecular Sciences. The author of the article were Buonsenso, Fabio; Ghirga, Francesca; Romeo, Isabella; Siani, Gabriella; Pilato, Serena; Quaglio, Deborah; Pierini, Marco; Botta, Bruno; Calcaterra, Andrea. The article conveys some information:

Many biol. active compounds feature low solubility in aqueous media and, thus, poor bioavailability. The formation of the host-guest complex by using calixarene-based macrocycles (i.e., resorcinol-derived cyclic oligomers) with a good solubility profile can improve solubilization of hydrophobic drugs. Herein, we explore the ability of resorc[4]arenes to self-assemble in polar solutions, to form supramol. aggregates, and to promote water-solubility of an isoflavone endowed with anti-cancer activity, namely Glabrescione B (GlaB). Accordingly, we synthesized several architectures featuring a different pattern of substitution on the upper rim including functional groups able to undergo acid dissociation (i.e., carboxyl and hydroxyl groups). The aggregation phenomenon of the amphiphilic resorc[4]arenes has been investigated in a THF/water solution by UV-visible spectroscopy, at different pH values. Based on their ionization properties, we demonstrated that the supramol. assembly of resorc[4]arene-based systems can be modulated at given pH values, and thus promoting the solubility of GlaB. In addition to this study using m-Methoxyphenol, there are many other studies that have used m-Methoxyphenol(cas: 150-19-6Application of 150-19-6) was used in this study.

m-Methoxyphenol(cas: 150-19-6) may be used as an analytical standard for the determination of the analyte in wine, coffee beans, wood samples, and mainstream smoke by gas chromatography (GC) based techniques.Application of 150-19-6

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

Rodrigues, Vereena’s team published research in Journal of Biosciences (New Delhi, India) in 2021 | CAS: 673-22-3

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is the main component of root bark essential oil of Periploca sepium Bunge. It is a potential tyrosinase inhibitor present in African medicinal plants. 2-Hydroxy-4-methoxybenzaldehyde was used in the synthesis of Schiff base ligand.Category: ethers-buliding-blocks

Category: ethers-buliding-blocksIn 2021 ,《Decalepis salicifolia (Bedd. ex Hook. f.) Venter: A steno-endemic and critically endangered medicinal and aromatic plant from Western Ghats, India》 appeared in Journal of Biosciences (New Delhi, India). The author of the article were Rodrigues, Vereena; Kumar, Amit; Gokul, Sivaraman; Shukla, Ashutosh K.; Ravikumar, Kaliamoorthy; Sundaresan, Velusamy. The article conveys some information:

A review.,. Decalepis salicifolia (Bedd. ex Hook. f.) Venter is a potential medicinal and highly aromatic plant species confined to the southernmost part of the Western Ghats of India. The plant is well known for its traditional uses among the various tribal communities of south India. The tubers of the plant possess characteristic vanillin-like aroma due to the presence of the compound 2-hydroxy-4-methoxybenzaldehyde. The tubers are used to substitute Hemidesmus indicus in various herbal formulations. The plants in the wild are continuously uprooted for their roots, leading to the irreversible destruction of the whole plant. The resulting tremendous loss of populations in the wild led to the species being declared as critically endangered by IUCN. Our group is working on the various aspects of this species including population status, distribution mapping, prospection, and conservation management. In the present , we have brought out the available information till date on D. salicifolia, including taxonomy, ethno-medicinal uses, phytochem., pharmacol., population status, and conservation efforts along with research gap and lacunae to provide direction for further research into this less explored medicinal and aromatic plant.2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3Category: ethers-buliding-blocks) was used in this study.

2-Hydroxy-4-methoxybenzaldehyde(cas: 673-22-3) is the main component of root bark essential oil of Periploca sepium Bunge. It is a potential tyrosinase inhibitor present in African medicinal plants. 2-Hydroxy-4-methoxybenzaldehyde was used in the synthesis of Schiff base ligand.Category: ethers-buliding-blocks

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