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N-(2-carboxybenzoyl)glutamic acid, also known as N-(2-carboxyphenyl)glutamic acid or 2-(N-carboxybenzoyl)glutamic acid, is a synthetic chemical compound with the molecular formula C12H11NO6. It is a derivative of glutamic acid, an amino acid that plays a crucial role in various biological processes. N-(2-carboxybenzoyl)glutamic acid features a carboxybenzoyl group attached to the nitrogen atom of the glutamic acid backbone, which can potentially influence its chemical properties and reactivity. It is often used in research and development for the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its unique structure and functional groups.

2353-40-4

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2353-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2353-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2353-40:
(6*2)+(5*3)+(4*5)+(3*3)+(2*4)+(1*0)=64
64 % 10 = 4
So 2353-40-4 is a valid CAS Registry Number.

2353-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(2-carboxybenzoyl)amino]pentanedioic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:2353-40-4 SDS

2353-40-4Downstream Products

2353-40-4Relevant academic research and scientific papers

Synthesis of 3-methylaspartic acids by ring-contraction of a nickelacycle derived from glutamic anhydride

Echavarren, Antonio M.,Castano, Ana M.

, p. 2369 - 2378 (1995)

The synthesis of protected methylaspartic acids from glutamic acid has been achieved by means of ring contraction of the derived nickelacycle followed by insertion of isocyanides.

Hydrolyzed metabolites of thalidomide: Synthesis and TNF-α production-inhibitory activity

Nakamura, Takanori,Noguchi, Tomomi,Miyachi, Hiroyuki,Hashimoto, Yuichi

, p. 651 - 654 (2008/02/08)

Putative hydrolyzed metabolites of thalidomide were prepared and characterized, and their inhibitory activity on tumor necrosis factor (TNF)-α production in the human monocytic leukemia cell line THP-1 was evaluated. α-(2-Carboxybenzamido)glutarimide was a more potent TNF-α production inhibitor than thalidomide.

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