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82344-53-4

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82344-53-4 Usage

Physical appearance

Yellow to brown crystalline powder

Use

Intermediate in the synthesis of dyes, pigments, and pharmaceuticals

Synthesis

Nitration of 2-(N,N-diacetylamino)toluene followed by acetylation

Toxicity

Toxic if ingested or inhaled

Hazard

Can cause irritation to the skin and eyes

Classification

Hazardous substance

Safety protocols

Should be stored and handled in accordance with proper safety protocols

Check Digit Verification of cas no

The CAS Registry Mumber 82344-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,4 and 4 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82344-53:
(7*8)+(6*2)+(5*3)+(4*4)+(3*4)+(2*5)+(1*3)=124
124 % 10 = 4
So 82344-53-4 is a valid CAS Registry Number.

82344-53-4SDS

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 N-Acetyl-N-(2-methyl-6-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names N,N-diacetyl-6-nitro-o-toluidine

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:82344-53-4 SDS

82344-53-4Relevant articles and documents

Synthesis of N-Acetylbenzimidazole Derivatives

Tanaka, Kenjiro,Shimazaki, Michiko,Murakami, Yasuoki

, p. 2714 - 2722 (2007/10/02)

For the structure determination of thiazolobenzimidazol-3(2H)-one derivatives (2 or 3) they were converted to the corresponding 1-acetylbenzimidazoles (4) by desulfurization.The latter compounds (4) were alternatively prepared by the cyclization of 2-aminoacetanilide derivatives (5) with CS2 in dimethylformamide (DMF), followed by desulfurization with Raney Ni.However, the reactions of 5 with ethyl orthoformate/H2SO4 in DMF gave a mixture of 4 and its acetyl-rearranged product (7).Keywords-acetyl group; rearrangement; thiazolobenzimidazol-3(2H)-one; N-acetylbenzimidazoles; ethyl orthoformate; carbon disulfide; desulfurization

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