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(+/-)-(2t-carboxy-4c-isopropyl-pyrrolidin-3r-yl)-acetic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92117-73-2

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92117-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92117-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,1 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92117-73:
(7*9)+(6*2)+(5*1)+(4*1)+(3*7)+(2*7)+(1*3)=122
122 % 10 = 2
So 92117-73-2 is a valid CAS Registry Number.

92117-73-2Downstream Products

92117-73-2Relevant academic research and scientific papers

Syntheses of (±)-α-isokainic acid and (±)-α- dihydroallokainic acid using a decarboxylative Ramberg-Ba?cklund reaction

Hodgson, David M.,Hachisu, Shuji,Andrews, Mark D.

, p. 1267 - 1270 (2005)

Total syntheses of (±)-α-isokainic acid and (±)-α-dihydroallokainic acid have been achieved via tandem radical addition-homoallylic rearrangement and a decarboxylative Ramberg-Ba?cklund reaction as the key steps.

Stereocontrolled syntheses of kainoid amino acids from 7-azabicyclo[2.2.1] heptadienes using tandem radical addition-homoallylic radical rearrangement

Hodgson, David M.,Hachisu, Shuji,Andrews, Mark D.

, p. 8866 - 8876 (2007/10/03)

N-Boc syn-7-(2-hydroxyethyl)-4-(alkyl or aryl)sulfonyl-2-azabicyclo[2.2.1] hept-5-enes serve as precursors in syntheses of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid 43, α-kainic acid 12, α-isokainic acid 14, and α-dihydroalloka

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