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N-benzoyl-DL-glutamic acid is a synthetic chemical compound with the molecular formula C13H13NO5. It is a derivative of glutamic acid, an amino acid, where the carboxylic acid group is esterified with benzoyl chloride, resulting in the formation of an amide bond. N-benzoyl-DL-glutamic acid is a white crystalline solid and is soluble in water, ethanol, and other organic solvents. N-benzoyl-DL-glutamic acid is used in various applications, including as a building block in the synthesis of pharmaceuticals, as a chiral auxiliary in asymmetric synthesis, and as a reagent in analytical chemistry. Its properties, such as its ability to form salts and its reactivity, make it a versatile compound in the field of organic chemistry.

6460-81-7

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6460-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6460-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,6 and 0 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6460-81:
(6*6)+(5*4)+(4*6)+(3*0)+(2*8)+(1*1)=97
97 % 10 = 7
So 6460-81-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H13NO5/c14-10(15)7-6-9(12(17)18)13-11(16)8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,16)(H,14,15)(H,17,18)

6460-81-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzamidopentanedioic acid

1.2 Other means of identification

Product number -
Other names N-benzoyl-DL-glutamic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6460-81-7 SDS

6460-81-7Relevant 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.

Beauveria bassiana ATCC 7159 contains an L-specific α-amino acid benzamidase

Holland, Herbert L.,Andreana, Peter R.,Salehzadeh-Asl, Reza,Van Vliet, Aaron,Ihasz, Nancy J.,Brown, Frances M.

, p. 667 - 672 (2007/10/03)

Biotransformation of a series of racemic N-benzoyl α-amino acids by the fungus Beauveria bassiana ATCC 7159 results in isolation of the corresponding D-amino acid benzamides in high enantiomeric purity and yield.

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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