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1,3-Benzenedicarboxamide, N,N'-bis(4-aminophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2658-06-2

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2658-06-2 Usage

Molecular weight

222.25 g/mol

Chemical structure

A 1,3-benzenedicarboxamide with two 4-aminophenyl groups attached to the nitrogen atoms

Classification

Human carcinogen

Usage

a. Production of dyes and pigments
b. Manufacturing of rubber and plastics

Regulatory status

Banned for commercial use in many countries due to carcinogenic properties

Exposure routes

Inhalation, ingestion, and skin contact

Health risks

Linked to bladder and other types of cancer in humans

Safety measures

Strict safety guidelines and regulations in place to limit exposure to this hazardous chemical

Check Digit Verification of cas no

The CAS Registry Mumber 2658-06-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,5 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2658-06:
(6*2)+(5*6)+(4*5)+(3*8)+(2*0)+(1*6)=92
92 % 10 = 2
So 2658-06-2 is a valid CAS Registry Number.

2658-06-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-N,3-N-bis(4-aminophenyl)benzene-1,3-dicarboxamide

1.2 Other means of identification

Product number -
Other names 4',4''-diaminoisophthalanilide

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:2658-06-2 SDS

2658-06-2Downstream Products

2658-06-2Relevant academic research and scientific papers

Desymmetrization reactions: A convenient synthesis of aromatic diamide diamines

Picard,Arnaud,Tisnès

, p. 1471 - 1478 (2001)

A two-step process for the synthesis of various diamide diamines derived from 1,n-diamino benzene compounds is described. The amidation reaction is simple, mild, involves readily available bis(N-acylthiazolidine-2-thione) derivatives as acylating agents and requires only stoichiometric equivalents of diamine and acylating agents.

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