103667-50-1 Usage
Description
(2S)-2-(5-benzoylthiophen-2-yl)propanoic acid is a chemical compound with a molecular formula of C16H14O3S. It is a yellow crystalline powder that is insoluble in water but soluble in organic solvents. (2S)-2-(5-benzoylthiophen-2-yl)propanoic acid is a derivative of 2-thiopheneacetic acid and is known for its potential anti-inflammatory and analgesic properties.
Uses
Used in Pharmaceutical Industry:
(2S)-2-(5-benzoylthiophen-2-yl)propanoic acid is used as an intermediate in the synthesis of various pharmaceuticals for its potential anti-inflammatory and analgesic properties. It aids in the development of new drugs for pain management and inflammation.
Used in Agrochemical Industry:
(2S)-2-(5-benzoylthiophen-2-yl)propanoic acid is used as a building block in the synthesis of agrochemicals, contributing to the development of effective products for agricultural applications.
Used in Organic Synthesis:
(2S)-2-(5-benzoylthiophen-2-yl)propanoic acid is used as a key component in the synthesis of other organic compounds and materials, thanks to the benzoyl group present in its molecule. This makes it a valuable asset in the field of organic chemistry for creating a variety of new substances with diverse applications.
Check Digit Verification of cas no
The CAS Registry Mumber 103667-50-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,6 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 103667-50:
(8*1)+(7*0)+(6*3)+(5*6)+(4*6)+(3*7)+(2*5)+(1*0)=111
111 % 10 = 1
So 103667-50-1 is a valid CAS Registry Number.
103667-50-1Relevant articles and documents
Synthesis of α-heteroarylpropanoic acid via asymmetric hydroformylation catalyzed by Rh(I)-(R,S)-BINAPHOS and the subsequent oxidation
Tanaka, Ryo,Nakano, Koji,Nozaki, Kyoko
, p. 8671 - 8676 (2008/03/12)
(Chemical Equation Presented) The asymmetric hydroformylation of vinyl heteroarenes (vinylfurans and vinylthiophenes) was investigated by using Rh(I)-BINAPHOS derivatives as a catalyst. The hydroformylation of vinylthiophenes 1 gave the corresponding branched aldehydes 2 with high enantiopurities as major products. Oxidation of the aldehydes 2 successfully afforded α-heteroarylpropanoic acids 4 in good yields. In addition, the aldehydes 2 were reduced to alcohols 5 without loss of enantiomeric excess.
