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(S)-3-methyl-3-phenylpentanoic acid, also known as (S)-α-methylbenzenepropanoic acid, is a chiral organic compound with the molecular formula C??H??O?. It is a derivative of pentanoic acid, featuring a methyl group (-CH?) and a phenyl group (C?H?) attached to the third carbon atom. (S)-3-methyl-3-phenylpentanoic acid is an enantiomer, with the "S" prefix indicating the (S)-configuration, which means the highest priority substituent (phenyl group) is on the left side when looking at the chiral center from the perspective of the lowest priority substituent (hydrogen). (S)-3-methyl-3-phenylpentanoic acid is a white crystalline solid and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals.

3968-72-7

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3968-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3968-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,9,6 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3968-72:
(6*3)+(5*9)+(4*6)+(3*8)+(2*7)+(1*2)=127
127 % 10 = 7
So 3968-72-7 is a valid CAS Registry Number.

3968-72-7Relevant academic research and scientific papers

Enantioselective synthesis of quaternary carbon stereogenic centers through copper-catalyzed conjugate additions of aryl- and alkylaluminum reagents to acyclic trisubstituted enones

Dabrowski, Jennifer A.,Villaume, Matthew T.,Hoveyda, Amir H.

supporting information, p. 8156 - 8159 (2013/08/23)

Acyclic quaternary carbons by conjugate addition: The first examples of catalytic enantioselective conjugate additions of aryl and alkyl units that generate acyclic all-carbon quaternary stereogenic centers have been developed (see scheme). The requisite

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