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N-carbamoyl-3-nitrobenzamide is a chemical compound with the molecular formula C8H7N3O4. It is an organic compound that features a benzene ring with a nitro group at the 3-position and a carbamoyl group at the nitrogen atom. N-carbamoyl-3-nitrobenzamide is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals, particularly as an intermediate in the production of various active ingredients. Its structure provides a foundation for further chemical modifications, making it a valuable building block in the development of new compounds with specific therapeutic or pesticidal properties.

6971-48-8

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6971-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6971-48-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,7 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6971-48:
(6*6)+(5*9)+(4*7)+(3*1)+(2*4)+(1*8)=128
128 % 10 = 8
So 6971-48-8 is a valid CAS Registry Number.

6971-48-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-carbamoyl-3-nitrobenzamide

1.2 Other means of identification

Product number -
Other names m-Nitro-benzoyl-harnstoff

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:6971-48-8 SDS

6971-48-8Downstream Products

6971-48-8Relevant academic research and scientific papers

Novel two-step, one-pot synthesis of primary acylureas

Xiao, Zili,Yang, Michael G.,Tebben, Andrew J.,Galella, Michael A.,Weinstein, David S.

experimental part, p. 5843 - 5844 (2010/11/05)

A new procedure for the synthesis of primary acylureas from cyanamide and a variety of carboxylic acids is described. Under mild reaction conditions, the products were obtained in good yield from commercially available starting materials.

Nucleophilic substitution of urea on aromatic carboxylic acids via phosphorylation

Prabhakaran, P V,S, Jayadev,Nema, S K,Rao, K V C

, p. 1072 - 1073 (2007/10/02)

The nucleophilic substitution reaction of urea on aromatic carboxylic acids has been carried out via phosphorylation.Five different carboxylureas have been synthesised in good yields and with high purity.This new route makes the existing corrosive acid chloride route easier and can be used as a general route for the preparation of any acid-urea substitution product.The products have been characterized by elemeental analyses and spectral data (IR, PMR and mass).

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