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4987-96-6

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4987-96-6 Usage

General Description

4,6-dinitrobenzene-1,3-diamine, also known as 1,3-diamino-2,4-dinitrobenzene, is a chemical compound that consists of a benzene ring with two amino groups (NH2) and two nitro groups (NO2) attached at specific positions. It is commonly used in the production of dyes, pharmaceuticals, and other organic compounds. The compound's chemical properties make it useful as a precursor in the synthesis of various industrial products, including hair dyes, pharmaceuticals, and explosives. Its toxic and mutagenic effects mean that it should be handled with caution and proper safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 4987-96-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,8 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4987-96:
(6*4)+(5*9)+(4*8)+(3*7)+(2*9)+(1*6)=146
146 % 10 = 6
So 4987-96-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H6N4O4/c7-3-1-4(8)6(10(13)14)2-5(3)9(11)12/h1-2H,7-8H2

4987-96-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-dinitrobenzene-1,3-diamine

1.2 Other means of identification

Product number -
Other names 4.6-Dinitro-1.3-diamino-benzol

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:4987-96-6 SDS

4987-96-6Relevant articles and documents

Process for the preparation of derivatives of tetraaminobenzene

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Page/Page column 18-19, (2012/04/04)

A process is provided for preparing complexes of 1,2,4,5-tetraminobenzene with an aromatic diacid. The process design eliminates costly intermediate drying and recrystallization steps. Handling of solid materials with possible skin sensitizing properties and toxicity is avoided, thereby eliminating human and environmental exposure.

INTEGRATED PROCESSES FOR THE PREPARATION OF HETEROCYCLIC AROMATIC POLYMER PRECURSORS

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Page/Page column 24-25, (2012/07/13)

An integrated process is provided for efficiently preparing 2, 4, 5-triaminothiophenol, starting; high purity salts thereof; and complexes of 2, 4, 5-triaminothiophenol with aromatic diacids, which are precursors for making polymer for high performance fibers. The process design eliminates several costly intermediate drying and recrystallization steps. The handling of solid materials with possible skin sensitizing properties and toxicity is avoided, thereby eliminating human and environmental exposure.

Process for the synthesis of 1,3-diamino-4,6-dinitrobenzene

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Page/Page column 6, (2011/12/13)

A process is provided for the preparation of 1,3-diamino-4,6-dinitrobenzene by amination of 1,3-dihalo-4,6-dinitrobenzene. The presence of water advantageously results in a highly pure product, free or essentially free of glycol ether impurities.

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