107073-27-8 Usage
General Description
[3-(1H-pyrrol-1-yl)-2-thienyl]methanol is a chemical compound with a molecular structure containing a pyrrole ring attached to a thienyl group. It is classified as an alcohol due to its methanol functional group. This chemical may have potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. The pyrrole moiety in the compound makes it a potentially bioactive compound, while the thienyl group can provide interesting electronic and optical properties. Further research on this compound may lead to the development of new drugs, pesticides, and materials with specific and targeted properties.
Check Digit Verification of cas no
The CAS Registry Mumber 107073-27-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,7 and 3 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 107073-27:
(8*1)+(7*0)+(6*7)+(5*0)+(4*7)+(3*3)+(2*2)+(1*7)=98
98 % 10 = 8
So 107073-27-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H9NOS/c11-7-9-8(3-6-12-9)10-4-1-2-5-10/h1-6,11H,7H2
107073-27-8Relevant 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.
