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4-[(cyanomethyl)amino]benzoic acid is an organic compound with the chemical formula C9H8N2O2. It is a derivative of benzoic acid, featuring a cyanomethylamino group attached to the 4-position of the benzene ring. 4-[(cyanomethyl)amino]benzoic acid is characterized by its potential reactivity due to the presence of the cyano group, which can participate in various chemical reactions such as addition, substitution, and condensation. It is a white crystalline solid and is used in the synthesis of pharmaceuticals and other organic compounds. The compound's properties, such as its melting point and solubility, can be influenced by the presence of the cyano and carboxyl groups, making it a versatile building block in organic chemistry.

6275-82-7

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6275-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6275-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,7 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6275-82:
(6*6)+(5*2)+(4*7)+(3*5)+(2*8)+(1*2)=107
107 % 10 = 7
So 6275-82-7 is a valid CAS Registry Number.

6275-82-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(cyanomethylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names AR2951

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:6275-82-7 SDS

6275-82-7Relevant academic research and scientific papers

Design and Synthesis of Iminosydnones for Fast Click and Release Reactions with Cycloalkynes

Riomet, Margaux,Decuypere, Elodie,Porte, Karine,Bernard, Sabrina,Plougastel, Lucie,Kolodych, Sergii,Audisio, Davide,Taran, Frédéric

supporting information, p. 8535 - 8541 (2018/05/30)

Emerging applications in the field of chemical biology are currently limited by the lack of bioorthogonal reactions allowing both removal and linkage of chemical entities on complex biomolecules. We recently discovered a novel reaction between iminosydnones and strained alkynes leading to two products resulting from ligation and fragmentation of iminosydnones under physiological conditions. We now report the synthesis of a panel of substituted iminosydnones and the structure reactivity relationship between these compounds and strained alkyne partners. This study identified the most relevant substituents, which allow to increase the rate of the transformation and to develop a bifunctional cleavable linker with improved kinetics.

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