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Benzoic acid, 2-(((2,6-dioxo-3-piperidinyl)amino)carbonyl)-, is a complex organic compound with the chemical formula C13H14N2O5. It is a derivative of benzoic acid, featuring a piperidine ring attached to the carboxylic acid group through an amide linkage. Benzoic acid,2-(((2,6-dioxo-3-piperidinyl)amino)carbonyl)- is known for its potential applications in pharmaceuticals, particularly as an intermediate in the synthesis of various drugs. Its structure includes a benzene ring with a carboxylic acid group at the 2-position and a piperidine ring connected through a carbonyl group, which contributes to its reactivity and functional group chemistry. The compound's properties, such as solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

6139-18-0

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6139-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6139-18-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6139-18:
(6*6)+(5*1)+(4*3)+(3*9)+(2*1)+(1*8)=90
90 % 10 = 0
So 6139-18-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O5/c16-10-6-5-9(12(18)15-10)14-11(17)7-3-1-2-4-8(7)13(19)20/h1-4,9H,5-6H2,(H,14,17)(H,19,20)(H,15,16,18)

6139-18-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name α-(o-Carboxybenzamido) glutarimide

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

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

More Details:6139-18-0 SDS

6139-18-0Downstream Products

6139-18-0Relevant academic research and scientific papers

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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