914348-82-6 Usage
General Description
2-(4-Methoxyphenyl)thiazole-5-carbaldehyde is a chemical compound with the molecular formula C11H9NOS and a molecular weight of 207.26 g/mol. It is a thiazole derivative with a carbonyl group and a methoxyphenyl group attached to the thiazole ring. 2-(4-METHOXYPHENYL)THIAZOLE-5-CARBALDEHYDE has potential applications in the pharmaceutical and agrochemical industries, as it can be used as a building block in the synthesis of various organic molecules. Its unique structure and reactivity make it a valuable intermediate for the production of biologically active compounds and materials with specific properties. Furthermore, it can also be used in research laboratories for organic synthesis and chemical analysis. Overall, 2-(4-Methoxyphenyl)thiazole-5-carbaldehyde is a versatile chemical compound with a wide range of potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 914348-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,3,4 and 8 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 914348-82:
(8*9)+(7*1)+(6*4)+(5*3)+(4*4)+(3*8)+(2*8)+(1*2)=176
176 % 10 = 6
So 914348-82-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO2S/c1-14-9-4-2-8(3-5-9)11-12-6-10(7-13)15-11/h2-7H,1H3
914348-82-6Relevant 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.
