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4-[methyl(nitroso)amino]benzoic acid, also known as 4-(methylnitrosamino)benzoic acid or MNAB, is a chemical compound with the molecular formula C8H8N2O3. It is a derivative of benzoic acid, where a methylnitrosamine group is attached to the 4-position of the benzene ring. MNAB is an organic compound that belongs to the class of nitrosamines, which are known for their potential carcinogenic properties. The compound is characterized by its yellow crystalline appearance and is soluble in organic solvents. Due to its structural features, MNAB has been a subject of interest in chemical research, particularly in the study of nitrosamine formation and its implications in various industrial and environmental processes.

5757-76-6

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5757-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5757-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,5 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5757-76:
(6*5)+(5*7)+(4*5)+(3*7)+(2*7)+(1*6)=126
126 % 10 = 6
So 5757-76-6 is a valid CAS Registry Number.

5757-76-6SDS

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 4-[methyl(nitroso)amino]benzoic acid

1.2 Other means of identification

Product number -
Other names 4-<N-Methyl-nitrosamino>-benzoesaeure

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:5757-76-6 SDS

5757-76-6Downstream Products

5757-76-6Relevant academic research and scientific papers

Discovery of chemoselective and biocompatible reactions using a high-throughput immunoassay screening

Kolodych, Sergii,Rasolofonjatovo, Evelia,Chaumontet, Manon,Nevers, Marie-Claire,Creminon, Christophe,Taran, Frederic

supporting information, p. 12056 - 12060 (2013/12/04)

An immunoassay-based method was used to screen numerous combinations of dipoles and dipolarophiles for their ability to undergo chemoselective and biocompatible [3+2] cycloaddition reactions. The approach fulfills most of the requirements of the click concept and led to the discovery of a copper-catalyzed reaction that generates pyrazoles from sydnone and alkyne reagents. Copyright

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