Tag: 100-200

Facile synthesis of N-1,2,4-oxadiazole substituted sulfoximines from N-cyano sulfoximines was written by M. L., Chenna Reddy;Nawaz Khan, Fazlur Rahman;Saravanan, Vadivelu. And the article was included in Organic & Biomolecular Chemistry in 2019.Name: 2-(4-Methoxyphenoxy)acetic acid This article mentions the following:

A divergent approach has been successfully developed for synthesis of N-1,2,4-oxadiazole substituted sulfoximines starting from N-cyano sulfoximines. This method has a wide degree of substrate scope that includes aryl, heteroaryl, alkyl, fluoroalkyl and saturated heterocyclic compounds Excellent functional group tolerability was also observed Extension of this methodol. to nucleosides, amino acids and dipeptides was found to be successful. A gram scale reaction was also established. The major part of this method is metal free and the utility of environmentally friendly solvents such as 2-Me THF and ionic liquids is an added advantage. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Name: 2-(4-Methoxyphenoxy)acetic acid).

2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly autoxidize to form hydroperoxides and dialkyl peroxides. If concentrated or heated, these peroxides may explode. To prevent such explosions, ethers should be obtained in small quantities, kept in tightly sealed containers, and used promptly.Name: 2-(4-Methoxyphenoxy)acetic acid

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

Guided in Situ Polymerization of MEH-PPV in Mesoporous Titania Photoanodes was written by Minar, Norma K.;Docampo, Pablo;Fattakhova-Rohlfing, Dina;Bein, Thomas. And the article was included in ACS Applied Materials & Interfaces in 2015.Recommanded Product: 1877-75-4 This article mentions the following:

Incorporation of conjugated polymers into porous metal oxide networks is a challenging task, which is being pursued via many different approaches. We have developed the guided in situ polymerization of poly(2-methoxy-5-(2′-ethylhexyloxy)-p-phenylenevinylene) (MEH-PPV) in porous titania films by means of surface functionalization. The controlled polymerization via the Gilch route was induced by an alkoxide base and by increasing the temperature The selected and specially designed surface-functionalizing linker mols. mimic the monomer or its activated form, resp. In this way, we drastically enhanced the amount of MEH-PPV incorporated into the porous titania phase compared to nonfunctionalized samples by a factor of 6. Addnl., photovoltaic measurements were performed. The devices show shunting or series resistance limitations, depending on the surface functionalization prior to in situ polymerization of MEH-PPV. We suggest that the reason for this behavior can be found in the orientation of the grown polymer chains with respect to the titania surface. Therefore, the geometry of the anchoring via the linker mols. is relevant for exploiting the full electronic potential of the conjugated polymer in the resulting hybrid composite. This observation will help to design future synthesis methods for new hybrid materials from conjugated polymers and n-type semiconductors to take full advantage of favorable electronic interactions between the two phases. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Recommanded Product: 1877-75-4).

2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly autoxidize to form hydroperoxides and dialkyl peroxides. If concentrated or heated, these peroxides may explode. To prevent such explosions, ethers should be obtained in small quantities, kept in tightly sealed containers, and used promptly.Recommanded Product: 1877-75-4

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

Nonvolatile and nonflammable sulfolane-based electrolyte achieving effective and safe operation of the Li-O₂ battery in open O₂ environment was written by Li, Zhengang;Song, Cun;Dai, Peng;Wu, Xiaohong;Zhou, Shiyuan;Qiao, Yu;Huang, Ling;Sun, Shi-Gang. And the article was included in Nano Letters in 2022.HPLC of Formula: 112-49-2 This article mentions the following:

The Li-O₂ battery should operate effectively/safely in an open O₂ environment for practical applications, but not trapped in sealed/closed atm. However, the typical use of volatile and flammable electrolyte restricts Li-O₂ battery to be able to be running in open O₂ environment. We report herein, for the first time, a highly electrochem. reversible Li-O₂ battery operated in an open O₂ environment, i.e., under the condition of keeping O₂ flowing continuously based on a nonvolatile and nonflammable sulfolane (TMS) solvent. The electrochem. irreversibility of Li₂O₂/O₂ conversion and incompatibility between Li metal anodes and electrolyte have been addressed via dissolving LiNO₃ in concentrated TMS electrolyte. The tuned electrolyte not only enables a stable solid electrolyte interphase (SEI) with conformal inorganic components (including LiF, LiN_xO_y, and Li₂O) that promotes a uniform Li electro-plating/stripping process but also results in a low charge overpotential, a stable discharge terminal plateau, and reversible O₂ generation of the Li-O₂ battery conducted in an open O₂ environment. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2HPLC of Formula: 112-49-2).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. The oxygen atom in ethers are more electronegative than carbon, thus the hydrogens which are alpha to the ethers are more acidic than the simple hydrocarbons. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).HPLC of Formula: 112-49-2

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

The dehydrative etherification of benzyl alcohols via mechanochemical reaction was written by Bian, Meng-Hua;Lu, Li-Yu;Zhang, Pu;Guo, Zhi-Xin. And the article was included in Tetrahedron Letters in 2022.Quality Control of (4-Methoxyphenyl)methanol This article mentions the following:

A facile, solvent-free, lower-cost, and efficient high-speed ball milling reaction catalyzed by Cu(NO₃)₂璺?H₂O/P₂O₅ were developed for the synthesis of sym. ethers ArCH(R)OCH(R)Ar (R = H, Me, Et, Ph; Ar = 4-chlorophenyl, naphthalen-1-yl, thiophen-2-yl, etc.) and 1-(1,2,3,4-tetrahydronaphthalen-1-yloxy)-1,2,3,4-tetrahydronaphthalene from dehydration of benzyl alcs. ArCH(R)OH and 1,2,3,4-tetrahydronaphthalen-1-ol by taking a benzylic carbocation as intermediate. In the experiment, the researchers used many compounds, for example, (4-Methoxyphenyl)methanol (cas: 105-13-5Quality Control of (4-Methoxyphenyl)methanol).

(4-Methoxyphenyl)methanol (cas: 105-13-5) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. But on the other hand, ethers undergo cleavage by reaction with acids. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O閳ユ椊 or N閳ユ椊 bonds. 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.Quality Control of (4-Methoxyphenyl)methanol

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

Degradation and fate of fenitrothion applied to harvested rice grains was written by Takimoto, Yoshiyuki;Oshima, Masako;Miyamoto, Junshi. And the article was included in Nippon Noyaku Gakkaishi in 1978.Reference of 5367-32-8 This article mentions the following:

Studies were conducted on the fate of fenitrothion (I) [122-14-5] labeled with ¹⁴C at the meta Me group and applied to rice grains at 6 or 15 ppm after harvest. During rice storage at 30 and 15鎺? I was decomposed with half-lives of 4 and >12 mo, resp. Major decomposition products were the demethyl derivative (II) [21847-47-2] of I and 3-methyl-4-nitrophenol (III) [2581-34-2]. 3-Hydroxymethyl-4-nitrophenol [60463-12-9], P:S isomers and P:O analogs of both I and II, 4-methyl-5-nitropyrocatechol (IV) [68906-21-8], III Me ether [5367-32-8], and IV di-Me ether [7509-11-7], were formed in small amounts I and its decomposition products penetrated into the grains about 100 娓璵 in depth from the surface during 12 mo-storage. Milling removed approx. 60% of the applied ¹⁴C in rice. Cooking I-treated unpolished rice decomposed I mainly into II and III. Malathion (V) [121-75-5] in stored rice was decomposed at similar rates to those of I mainly into the demethyl derivative [68906-22-9] and V mono- and diacids. In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8Reference of 5367-32-8).

3-Methyl-4-nitroanisole (cas: 5367-32-8) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. Ethers can form hydrogen bonds with other molecules (alcohols, amines, etc.) that have O閳ユ椊 or N閳ユ椊 bonds. 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.Reference of 5367-32-8

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

Efficient cosubstrate enzyme pairs for sequence-specific methyltransferase-directed photolabile caging of DNA was written by Heimes, Michael;Kolmar, Leonie;Brieke, Clara. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2018.Application of 5367-32-8 This article mentions the following:

Supplemented with synthetic surrogates of their natural cosubstrate S-adenosyl-L-methionine (AdoMet), methyltransferases represent a powerful toolbox for the functionalization of biomols. By employing novel cosubstrate derivatives in combination with protein engineering, we show that this chemo-enzymic method can be used to introduce photolabile protecting groups into DNA even in the presence of AdoMet. This approach enables optochem. control of gene expression in a straight-forward manner and we have termed it reversible methyltransferase directed transfer of photoactivatable groups (re-mTAG). In the experiment, the researchers used many compounds, for example, 3-Methyl-4-nitroanisole (cas: 5367-32-8Application of 5367-32-8).

3-Methyl-4-nitroanisole (cas: 5367-32-8) belongs to ethers. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.Application of 5367-32-8

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

Asymmetric Vesicles Self-Assembled by Amphiphilic Sequence-Controlled Polymers was written by Huang, Pei;Qi, Meiwei;Chen, Chuanshuang;Xu, Fugui;Li, Shanlong;Xu, Qingsong;Pan, Hui;Wang, Yuling;Yu, Chunyang;Zhang, Shaodong;Zhou, Yongfeng. And the article was included in ACS Macro Letters in 2021.Product Details of 111-77-3 This article mentions the following:

The asym. distribution of lipids on the inner and outer membranes of a cell plays a pivotal role in the physiol. and immunol. activities of life. It has inspired the elaboration of synthetic asym. vesicles for the discovery of advanced materials and functions. The asym. vesicles were generally prepared by amphiphilic block copolymers. We herein report on the formation of asym. vesicles self-assembled by amphiphilic sequence-controlled polymers with two hydrophilic segments SU and TEO. We also developed an efficient fluorescence titration method with europium(III) ions (Eu³⁺) to determine the uneven distribution of SU and TEO. SU units are preferentially located on the outer membrane and TEO on the inner membrane of the resulting vesicles, which is facilitated by the electrostatic repulsion of SU and the U-shaped folding of the hydrophobic backbone of the resulting polymers. This work shows that sequence-controlled polymers with alternating monomer sequence provide a powerful toolbox for the elaboration of important yet challenging self-assembled structures for emerging functions and properties. In the experiment, the researchers used many compounds, for example, 2-(2-Methoxyethoxy)ethanol (cas: 111-77-3Product Details of 111-77-3).

2-(2-Methoxyethoxy)ethanol (cas: 111-77-3) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Product Details of 111-77-3

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

Discovery of an Oral, Rule of 5 Compliant, Interleukin 17A Protein-Protein Interaction Modulator for the Potential Treatment of Psoriasis and Other Inflammatory Diseases was written by Andrews, Mark D.;Dack, Kevin N.;de Groot, Marcel J.;Lambert, Maja;Sennbro, Carl J.;Larsen, Mogens;Stahlhut, Martin. And the article was included in Journal of Medicinal Chemistry in 2022.COA of Formula: C8H10O2 This article mentions the following:

Interleukin 17A (IL-17A) was an interleukin cytokine whose dysregulation implicated in autoimmune disorders such as psoriasis and monoclonal antibodies against the IL-17A pathway were now well-established and very effective treatments. Overlap of early ligands led to a series of benzhydrylglycine-containing compounds I [R¹ = C(O)N(Me)₂, pyrazol-4-yl, 3,5-(Me)₂-pyrazol-4-yl, etc.; R² = cyclopropyl, cyclohexyl, Ph, etc.; R³ = H, cyclopropyl Ph, etc.; R²R³ = Ph, cyclohexyl, cycloheptyl, etc.; R⁴ = Me, Et, iPr] that allowed foridentifying dimethylpyrazole as a key substituent that gave moderately potent PPIm with good oral bioavailability. Finally, optimization of the terminal amide group led to the identification of PPIm I [R¹ = 3,5-(Me)₂-pyrazol-4-yl; R² = cyclopropyl; R³ = cyclopropyl; R⁴ = iPr] as a clin. development candidate with the potential to be an oral treatment of IL-17A-mediated diseases. Protein crystallog. provided knowledge of the key binding interactions between small-mol. ligands and the IL-17A dimer and this helped in the multiparameter optimization toward identifying an orally bioavailable, Rule of 5 compliant PPIm of IL-17A. Exploration of the amino acid portion of the structure then led to dicyclopropylalanine as a group that gave potent and metabolically stable compounds, including the development candidate I [R¹ = 3,5-(Me)₂-pyrazol-4-yl; R² = cyclopropyl; R³ = cyclopropyl; R⁴ = iPr]. In the experiment, the researchers used many compounds, for example, (4-Methoxyphenyl)methanol (cas: 105-13-5COA of Formula: C8H10O2).

(4-Methoxyphenyl)methanol (cas: 105-13-5) belongs to ethers. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides. Ethyl ether is an excellent solvent for extractions and for a wide variety of chemical reactions. It is also used as a volatile starting fluid for diesel engines and gasoline engines in cold weather. Dimethyl ether is used as a spray propellant and refrigerant. Methyl t-butyl ether (MTBE) is a gasoline additive that boosts the octane number and reduces the amount of nitrogen-oxide pollutants in the exhaust. The ethers of ethylene glycol are used as solvents and plasticizers.COA of Formula: C8H10O2

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

Efficacy of stabilizing calcium battery electrolytes through salt-directed coordination change was written by Hahn, Nathan T.;McClary, Scott A.;Landers, Alan T.;Zavadil, Kevin R.. And the article was included in Journal of Physical Chemistry C in 2022.SDS of cas: 112-49-2 This article mentions the following:

Achieving practical, high-energy-d. calcium batteries requires controlling the stability of Ca²⁺ electrolytes during calcium metal cycling. Because of the highly reactive nature of calcium, most typical electrolyte constituents are unstable, leading to electrode passivation and low Coulombic efficiency. Among various com. available salts, calcium bis(trifluoromethylsulfonyl)imide (Ca(TFSI)₂) is attractive because of its oxidative stability and high solubility in a variety of solvents. However, this salt does not allow for calcium metal plating, and it has been proposed that TFSI^– instability induced by Ca²⁺ coordination is to blame. In this work, we test the ability of strongly coordinating Ca²⁺ cosalts such as halides and borohydrides to displace TFSI^– from the first coordination shell of Ca²⁺ and thereby stabilize TFSI-based electrolytes to enable calcium plating. Through spectroscopic anal., we find that the effectiveness of these cosalts at displacing the TFSI^– anion is dependent on the solvent’s coordination strength toward Ca²⁺. Surprisingly, electrochem. calcium deposition behavior is not correlated to the population of bound or free TFSI^–. Instead, the nature of the coordination interaction between Ca²⁺ and the cosalt anion is more important for determining stability. Our findings indicate that TFSI^– anions are inherently unstable during calcium deposition even in the nominally free state. Therefore, strategies aimed at eliminating the interactions of these anions with the electrode surface via interface/interphase design are required. In the experiment, the researchers used many compounds, for example, 2,5,8,11-Tetraoxadodecane (cas: 112-49-2SDS of cas: 112-49-2).

2,5,8,11-Tetraoxadodecane (cas: 112-49-2) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. At room temperature, ethers are pleasant-smelling colourless liquids. Relative to alcohols, ethers are generally less dense, are less soluble in water, and have lower boiling points. They are relatively unreactive, and as a result they are useful as solvents for fats, oils, waxes, perfumes, resins, dyes, gums, and hydrocarbons. Vapours of certain ethers are used as insecticides, miticides, and fumigants for soil.SDS of cas: 112-49-2

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

Study on the removal and depolymerization of lignin from corn stover through the synergistic effect of Bronsted acid, Lewis acid and hydrogenation sites was written by Zhang, Baikai;Li, Wenzhi;Zhang, Tingwei;Li, Xu;Ogunbiyi, Ajibola T.;Chen, Kun;Shen, Changcheng. And the article was included in Fuel in 2021.Electric Literature of C11H16O3 This article mentions the following:

The effective transformation of lignin is an essential part of realizing the comprehensive utilization of biomass. In this study, a one-pot method for the depolymerization of corn stover lignin used aluminum phosphate (NiAPO-5) zeolite catalyst contained Bronsted acid, Lewis acid and hydrogenation sites was proposed. It was found that the number of Bronsted acid sites was increased after NiAPO-5 was reduced with H₂. The yield of monomers and residue were 35.70% and 38.09% at 235鎺矯 for 3 h, resp. The result of 2D HSQC NMR showed that the NiAPO-5 (H₂) catalyst significantly affected the cleavage of 灏?O-4 bonds. The distribution of products and the stability of catalyst revealed that NiAPO-5 (H₂) was an efficient catalyst for the depolymerization of lignin. In the experiment, the researchers used many compounds, for example, 3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3Electric Literature of C11H16O3).

3-(3,4-Dimethoxyphenyl)propan-1-ol (cas: 3929-47-3) belongs to ethers. Of all the functional groups, ethers are the least reactive ones. Ether bonds are quite stable towards bases, oxidizing agents and reducing agents. Electron-deficient reagents are also stabilized by ethers. For example, borane (BH3) is a useful reagent for making alcohols. Pure borane exists as its dimer, diborane (B2H6), a toxic gas that is inconvenient and hazardous to use. Borane forms stable complexes with ethers, however, and it is often supplied and used as its liquid complex with tetrahydrofuran (THF).Electric Literature of C11H16O3

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