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130597-56-7

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130597-56-7 Usage

General Description

4-(Chloromethyl)-N-methyl-2-nitroaniline is a chemical compound with the molecular formula C8H9ClN2O2. It is a yellow crystalline solid with a molecular weight of 204.62 g/mol. 4-(Chloromethyl)-N-methyl-2-nitroaniline is commonly used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also used in the manufacturing of dyes and pigments. 4-(Chloromethyl)-N-methyl-2-nitroaniline is considered to be a hazardous substance and should be handled and stored with caution due to its potential health and environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 130597-56-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,9 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130597-56:
(8*1)+(7*3)+(6*0)+(5*5)+(4*9)+(3*7)+(2*5)+(1*6)=127
127 % 10 = 7
So 130597-56-7 is a valid CAS Registry Number.

130597-56-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Chloromethyl)-N-methyl-2-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,4-(chloromethyl)-N-methyl-2-nitro

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:130597-56-7 SDS

130597-56-7Downstream Products

130597-56-7Relevant articles and documents

Artificial redox enzymes

-

, (2008/06/13)

Artificial redox enzymes are disclosed wherein one or more redox coenzymes or cofactors are linked to the 2-O, 3-O or 6-O positions of a D-glucopyranose ring of α-, β-, or γ-cyclodextrins. Also disclosed are facile synthetic methods for producing said art

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