127641-48-9 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-(4-chlorophenyl)isovaleric acid methyl ester is used as an intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and medications.
Used in Chemical Research and Development:
As a building block, (S)-2-(4-chlorophenyl)isovaleric acid methyl ester is utilized in the production of other organic compounds, playing a crucial role in chemical research and development.
Used in Organic Compounds Production:
(S)-2-(4-chlorophenyl)isovaleric acid methyl ester serves as a valuable component in the creation of a wide range of organic compounds, showcasing its versatility and importance in the chemical industry.
Safety Note:
It is essential to handle (S)-2-(4-chlorophenyl)isovaleric acid methyl ester with care and follow proper safety protocols due to its potential hazards, ensuring the safety of individuals involved in its production, use, and research.
Check Digit Verification of cas no
The CAS Registry Mumber 127641-48-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,6,4 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127641-48:
(8*1)+(7*2)+(6*7)+(5*6)+(4*4)+(3*1)+(2*4)+(1*8)=129
129 % 10 = 9
So 127641-48-9 is a valid CAS Registry Number.
127641-48-9Relevant academic research and scientific papers
Process for preparing (S)- alpha-cyano-3-phenoxybenzyl-(S)-2-(4-chlorophenyl)-isovalerate
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Page/Page column 9; 12; 13, (2008/06/13)
The present invention relates to an environmentally benign process for the preparation of (S)-α-cyano-3-phenoxybenzyl-(S)-2-(4-chlorophenyl)isovalerate from its diastereomeric mixture (RS)-α-cyano-3-phenoxybenzyl-(S)-2-(4-chlorophenyl) isovalerate.
ENZYMATIC RESOLUTION OF METHYL 2-ALKYL-2-ARYLACETATES
Ahmar, M.,Girard, C.,Bloch, R.
, p. 7053 - 7056 (2007/10/02)
Horse liver esterase, used as its inexpensive commercial acetone powder, catalyzes the selective hydrolysis of methy 2-alkyl-2-arylacetates to afford R(-)-2-alkyl-2-arylacetic acids and S(+)-methyl 2-alkyl-2-arylacetates.
