937668-37-6 Usage
Description
[2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol is a chemical compound that belongs to the group of thiazole derivatives. It is characterized by a thiazole ring with a methoxyphenyl group attached to it, along with a methanol substituent. [2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol has been studied for its potential pharmaceutical and medicinal applications due to its wide range of biological activities, which include antimicrobial, antifungal, and anti-inflammatory properties. The methoxyphenyl group in this compound may also contribute to its pharmacological activity, as methoxy substituents are known to influence the chemical and biological properties of organic molecules.
Uses
Used in Pharmaceutical Applications:
[2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol is used as a potential pharmaceutical compound for its demonstrated antimicrobial, antifungal, and anti-inflammatory properties. [2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol's unique molecular structure, which includes a methoxyphenyl group, may enhance its effectiveness in treating various conditions and diseases.
Used in Drug Discovery and Development:
[2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol is used as a compound of interest in drug discovery and development. Its diverse biological activities and the potential influence of the methoxyphenyl group on its pharmacological properties make it a promising candidate for further research and characterization. This could lead to the development of new drugs with improved efficacy and safety profiles.
Used in Medicinal Chemistry Research:
[2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol is used as a subject of study in medicinal chemistry research. [2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol's structure and properties make it a valuable tool for understanding the relationship between molecular structure and biological activity, which is crucial for the design and development of new therapeutic agents.
Used in Chemical Synthesis:
[2-(4-Methoxyphenyl)-1,3-thiazol-5-yl]methanol may also be used as a building block or intermediate in the synthesis of more complex organic molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its unique structure and functional groups make it a versatile starting material for the development of novel compounds with tailored properties.
Check Digit Verification of cas no
The CAS Registry Mumber 937668-37-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,6,6 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 937668-37:
(8*9)+(7*3)+(6*7)+(5*6)+(4*6)+(3*8)+(2*3)+(1*7)=226
226 % 10 = 6
So 937668-37-6 is a valid CAS Registry Number.
937668-37-6Relevant articles and documents
Metal-Free Aerobic Oxidative Selective C-C Bond Cleavage in Heteroaryl-Containing Primary and Secondary Alcohols
Xia, Anjie,Qi, Xueyu,Mao, Xin,Wu, Xiaoai,Yang, Xin,Zhang, Rong,Xiang, Zhiyu,Lian, Zhong,Chen, Yingchun,Yang, Shengyong
supporting information, (2019/05/07)
A transition-metal-free aerobic oxidative selective C-C bond-cleavage reaction in primary and secondary heteroaryl alcohols is reported. This reaction was highly efficient and tolerated various heteroaryl alcohols, generating a carboxylic acid derivative and a neutral heteroaromatic compound. Experimental studies combined with density functional theory calculations revealed the mechanism underlying the selective C-C bond cleavage. This strategy also provides an alternative simple approach to carboxylation reaction.
