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57610-10-3

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57610-10-3 Usage

General Description

2-Nitroso-5-nitrotoluene is a chemical compound with the molecular formula C7H6N2O3. It is a yellow crystalline solid that is primarily used in the production of dyes and pigments. It is also known to have some potential applications in the pharmaceutical industry. The compound is considered to be toxic and harmful if ingested or inhaled, and can cause irritation to the skin and eyes. Additionally, it is a known carcinogen and should be handled with caution. Its chemical properties include it being insoluble in water and having a high melting point. Despite its potential uses, the compound's toxic nature and potential health hazards make it a substance that requires careful handling and consideration.

Check Digit Verification of cas no

The CAS Registry Mumber 57610-10-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,6,1 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 57610-10:
(7*5)+(6*7)+(5*6)+(4*1)+(3*0)+(2*1)+(1*0)=113
113 % 10 = 3
So 57610-10-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N2O3/c1-5-4-6(9(11)12)2-3-7(5)8-10/h2-4H,1H3

57610-10-3SDS

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 2-methyl-4-nitro-1-nitrosobenzene

1.2 Other means of identification

Product number -
Other names 2-nitroso-5-nitrotoluene

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:57610-10-3 SDS

57610-10-3Relevant articles and documents

Oxidation of Primary Aromatic Amines, Catalyzed by Tungsten Compounds

Mel'nikov, E. B.,Suboch, G. A.,Belyaev, E. Yu.

, p. 1640 - 1642 (2007/10/03)

Treatment of o-nitroanilines and o-aminobenzoic acids with 30 percent hydrogen peroxide in the presence of Na2WO4 and H3PO4 results in selective formation of corresponding nitroso derivatives.In other cases, the products are azoxy compounds.Oxidation of anilines containing alkyl or alkoxy groups in the ortho and para positions with hydrogen peroxide in the presence of Na2WO4 and tetrabutylammonium bromide quantitatively yields corresponding nitrosobenzenes.The H2O2-Na2WO4-H3PO4 system in the presence of tetrabutylammonium bromide is proposed for preparation of nitroso derivatives from anilines containing electron-acceptor meta and para substituents.

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