317319-36-1 Usage
General Description
{2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol is a chemical compound that belongs to the class of thiazole derivatives. It is composed of a thiazole ring with a fluorinated benzene ring and a methyl group. The presence of the fluorine and trifluoromethyl groups in the benzene ring makes this compound potentially useful in medicinal chemistry as it can modulate the biological activity of the molecule. The hydroxyl group attached to the thiazole ring makes it a potential candidate for drug development as it can serve as a hydrogen bond donor or acceptor in binding to target proteins. {2-[2-fluoro-4-(trifluoromethyl)phenyl]-4-methyl-1,3-thiazol-5-yl}methanol has potential applications in the pharmaceutical industry as a building block in the synthesis of various drugs due to its interesting structural features.
Check Digit Verification of cas no
The CAS Registry Mumber 317319-36-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,7,3,1 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 317319-36:
(8*3)+(7*1)+(6*7)+(5*3)+(4*1)+(3*9)+(2*3)+(1*6)=131
131 % 10 = 1
So 317319-36-1 is a valid CAS Registry Number.
317319-36-1Relevant articles and documents
Process development for sodelglitazar: A ppar panagonist
Brown, Andrew D.,Davis, Roman D.,Fitzgerald, Russ N.,Glover, Bobby N.,Harvey, Kim A.,Jones, Lynda A.,Liu, Bing,Patterson, Daniel E.,Sharp, Matthew J.
experimental part, p. 297 - 302 (2010/04/22)
Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier syntheses. This process produces sodelglitazar in 74% overall yield from readily available thiophenol (8) and thiazole alcohol (3).
