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CAS

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2658-07-3

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

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  • 2658-07-3 Structure

  • Basic information

    1. Product Name: 1,3-Benzenedicarboxamide, N,N'-bis(3-aminophenyl)-
    2. Synonyms:
    3. CAS NO:2658-07-3
    4. Molecular Formula: C20H18N4O2
    5. Molecular Weight: 346.389
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 2658-07-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,3-Benzenedicarboxamide, N,N'-bis(3-aminophenyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,3-Benzenedicarboxamide, N,N'-bis(3-aminophenyl)-(2658-07-3)
    11. EPA Substance Registry System: 1,3-Benzenedicarboxamide, N,N'-bis(3-aminophenyl)-(2658-07-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 2658-07-3(Hazardous Substances Data)

2658-07-3 Usage

Chemical Structure

A derivative of benzene with two amine groups attached to the benzene ring

Composition

Contains carbon, hydrogen, nitrogen, and oxygen atoms

Functional Groups

Amine (-NH2) and carboxamide (-CONH2) groups

Applications

a. Manufacturing of polymers, plastics, and fibers
b. Production of agricultural products
c. Building block for pharmaceutical compounds

High thermal stability

Resistant to high temperatures, making it suitable for various industrial applications

Mechanical strength

Exhibits strong structural properties, contributing to its versatility in different industries

Appearance

Typically a solid or crystalline substance

Solubility

Soluble in polar solvents such as water and alcohol

Reactivity

Can undergo various chemical reactions, such as substitution, addition, and condensation, due to the presence of amine and carboxamide functional groups

Safety

Handle with care, as it may have potential health risks and should be stored and used according to safety guidelines

Environmental Impact

May have an impact on the environment if not disposed of or used properly, so proper waste management and recycling practices should be followed

Check Digit Verification of cas no

The CAS Registry Mumber 2658-07-3 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 2658-07:
(6*2)+(5*6)+(4*5)+(3*8)+(2*0)+(1*7)=93
93 % 10 = 3
So 2658-07-3 is a valid CAS Registry Number.

2658-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 1,3-Benzenedicarboxamide,N,N'-bis(3-aminophenyl)

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:2658-07-3 SDS

2658-07-3Relevant articles and documents

Ring-chain interconversion in high-performance polymer systems. 3. Cyclodepolymerization of poly(m-phenylene isophthalamide) (nomex) and entropically driven ring-opening polymerization of the macrocyclic oligomers so produced

Ben-Haida, Abderrazak,Hodge, Philip,Colquhoun, Howard M.

, p. 722 - 729 (2007/10/03)

A homologous series of macrocyclic oligoamides has been prepared in high yield by reaction of isophthaloyl chloride with m-phenylenediamine under pseudo-high-dilution conditions. The products were characterized by infrared and 1H NMR spectrosco

Desymmetrization reactions: A convenient synthesis of aromatic diamide diamines

Picard,Arnaud,Tisnès

, p. 1471 - 1478 (2007/10/03)

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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