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(R,S)-N-benzoyl-2-aminoadipic acid is a chiral compound with the molecular formula C13H15NO4. It is a derivative of 2-aminoadipic acid, where the amino group is acylated with a benzoyl group. (R,S)-N-benzoyl-2-aminoadipic acid is significant in organic chemistry and pharmaceutical research due to its potential applications in the synthesis of various biologically active molecules and as a building block for the development of new drugs. The presence of both R and S configurations indicates that it is a mixture of two enantiomers, which can have different biological activities and properties. Understanding the stereochemistry and reactivity of such compounds is crucial for their effective use in medicinal chemistry and the creation of enantiomerically pure drugs.

91958-56-4

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91958-56-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91958-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,5 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 91958-56:
(7*9)+(6*1)+(5*9)+(4*5)+(3*8)+(2*5)+(1*6)=174
174 % 10 = 4
So 91958-56-4 is a valid CAS Registry Number.

91958-56-4Relevant academic research and scientific papers

Discovery of a novel class of 1,3-dioxane-2-carboxylic acid derivatives as subtype-selective peroxisome proliferator-activated receptor α (PPARα) agonists

Aoki, Tomiyoshi,Asaki, Tetsuo,Hamamoto, Taisuke,Sugiyama, Yukiteru,Ohmachi, Shinji,Kuwabara, Kenji,Murakami, Kohji,Todo, Makoto

, p. 2128 - 2132 (2008/12/21)

A new series of 1,3-dioxane-2-carboxylic acid derivatives was synthesized and evaluated for agonist activity at human peroxisome proliferator-activated receptor (PPAR) subtypes. Structure-activity relationship studies led to the identification of 2-methyl-c-5-[4-(5-methyl-2-phenyl-1,3-oxazol-4-yl)butyl]-1,3-dioxane-r-2-carboxylic acid 4b as a potent PPARα agonist with high subtype selectivity at human receptor subtypes. This compound exhibited a substantial hypolipidemic effect in type 2 diabetic KK-Ay mice.

Asymmetric Catalysis by Vitamin B12: The Isomerization of Achiral Aziridines to Optically Active Allylic Amines

Zhang, Zhong da,Scheffold, Rolf

, p. 2602 - 2615 (2007/10/02)

Achiral N-acylaziridines are isomerized to optically active N-acyl-allylamines in ee's of up to 95percent by catalytic amounts of cob(I)alamin in MeOH.

Composition containing a penem or carbapenem antibiotic

-

, (2008/06/13)

Administration of an N-acylated amino acid in association with a penem or carbapenem antibiotic relieves or eliminates the renal problems associated with administration of the antibiotic alone. The amino acid derivative and antibiotic may be formulated together as a composition or administered separately, either simultaneously or sequentially. The composition may be prepared by simple mixing.

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