71455-51-1 Usage
General Description
4-(4-chloro-benzoylamino)-butyric acid is a chemical compound with the molecular formula C11H12ClNO3. It is a derivative of butyric acid and contains a benzoylamino group and a chlorine atom. 4-(4-CHLORO-BENZOYLAMINO)-BUTYRIC ACID has potential applications in pharmaceuticals and as a building block in organic synthesis. It may possess biological activities and is under investigation for potential therapeutic uses. The specific properties and uses of 4-(4-chloro-benzoylamino)-butyric acid are still being studied, and it has the potential to be a valuable compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 71455-51-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,5 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 71455-51:
(7*7)+(6*1)+(5*4)+(4*5)+(3*5)+(2*5)+(1*1)=121
121 % 10 = 1
So 71455-51-1 is a valid CAS Registry Number.
InChI:InChI=1/C11H12ClNO3/c12-9-5-3-8(4-6-9)11(16)13-7-1-2-10(14)15/h3-6H,1-2,7H2,(H,13,16)(H,14,15)/p-1
71455-51-1Relevant articles and documents
Aryl carboxylic acid reduction and further reactions with GABA and glucose promoted by whole cells of Xylaria arbuscula
Amaral, Luciana Da Silva,Rodrigues-Filho, Edson
, p. 90 - 94 (2015/02/19)
Xylaria arbuscula was collected from a Cypress tree, Cupressus lusitanica. The whole cells of this endophytic fungus were used in screening for microbial bioreduction of aryl acids. Different p-substituted benzoic acids were evaluated. However, only p-bromobenzoic acid, p-chlorobenzoic acid and p-nitrobenzoic acid were converted to their corresponding alcohols. Aryl acid metabolism of X. arbuscula included GABA incorporation and glycosylation when the substrates were p-bromobenzoic and p-chlorobenzoic acids were also observed. The substrates p-hydroxybenzoic and p-aminobenzoic acids were not transformed. These results could suggest that electron-withdrawing groups at para orientation activate the substrate for reduction.
