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Benzamide, N-methyl-N-(2-nitrophenyl)-, also known as N-Methyl-2-Nitrophenylbenzamide, is an organic compound with the chemical formula C14H12N2O3. It is a derivative of benzamide, featuring a nitro group (NO2) attached to the 2-position of the phenyl ring and a methyl group (CH3) attached to the nitrogen atom. This yellow crystalline solid is soluble in organic solvents and has a molecular weight of 256.26 g/mol. It is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical compounds. Due to its reactivity and potential applications, it is essential to handle Benzamide, N-methyl-N-(2-nitrophenyl)- with care, following proper safety protocols.

5496-57-1

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5496-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5496-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,9 and 6 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5496-57:
(6*5)+(5*4)+(4*9)+(3*6)+(2*5)+(1*7)=121
121 % 10 = 1
So 5496-57-1 is a valid CAS Registry Number.

5496-57-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-(2-nitrophenyl)benzamide

1.2 Other means of identification

Product number -
Other names 2'-Nitro-N-methylbenzanilide

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:5496-57-1 SDS

5496-57-1Downstream Products

5496-57-1Relevant academic research and scientific papers

Nitration of the Acetanilide-type Compounds

Daszkiewicz, Zdzislaw,Kyziol, Janusz B.

, p. 44 - 50 (2007/10/02)

Some aromatic compounds containing the imino group (NH) were nitrated in acetic acid or anhydride, and the ortho/para ratios were measured.N-Methyl derivatives of the aforementioned compounds are much less reactive when nitrated under comparable conditions and give significantly lower o/p ratios.These results along with the literature data support the hypothesis that the acetanilide-type compounds are nitrated via N-nitro intermediates.

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