103667-49-8 Usage
Description
(2R)-2-(5-benzoylthiophen-2-yl)propanoic acid is a chiral chemical compound with the molecular formula C17H14O3S. It features a thiophene ring connected to a propanoic acid moiety, with an additional benzoyl group attached to the thiophene ring. (2R)-2-(5-benzoylthiophen-2-yl)propanoic acid has potential applications in the pharmaceutical industry due to its unique structure and may exhibit biological activity.
Uses
Used in Pharmaceutical Industry:
(2R)-2-(5-benzoylthiophen-2-yl)propanoic acid is used as a starting material in organic synthesis for the production of other compounds with similar structures and properties. Its unique molecular structure may contribute to the development of new pharmaceuticals with potential biological activity.
Used in Organic Synthesis:
(2R)-2-(5-benzoylthiophen-2-yl)propanoic acid is used as a building block in the synthesis of various organic compounds. Its versatile structure allows for the creation of new molecules with potential applications in different fields, including pharmaceuticals, materials science, and chemical research.
It is important to handle (2R)-2-(5-benzoylthiophen-2-yl)propanoic acid with care, as it may have specific hazards associated with its use and manipulation. Proper safety measures should be taken to ensure the safe handling and storage of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 103667-49-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103667-49:
(8*1)+(7*0)+(6*3)+(5*6)+(4*6)+(3*7)+(2*4)+(1*9)=118
118 % 10 = 8
So 103667-49-8 is a valid CAS Registry Number.
103667-49-8Relevant 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 (2007)
(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.
