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1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 143586-51-0 Structure
  • Basic information

    1. Product Name: 1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]-
    2. Synonyms:
    3. CAS NO:143586-51-0
    4. Molecular Formula: C24H24N2O4
    5. Molecular Weight: 404.466
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 143586-51-0.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: 1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]-(143586-51-0)
    11. EPA Substance Registry System: 1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]-(143586-51-0)
  • 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: 143586-51-0(Hazardous Substances Data)

143586-51-0 Usage

Chemical compound

1,2-Benzenediamine, N,N'-bis[(3,4-dimethoxyphenyl)methylene]-

Type

Diamine derivative

Applications

a. Production of dyes and pigments
b. Metal complex chemistry (formation of coordination compounds with various metal ions)
c. Synthesis of organic materials
d. Ligand in catalysis reactions

Properties

a. Aromatic (due to the presence of benzene rings)
b. Amine (due to the presence of amine groups)
c. Wide range of industrial and research applications

Structure

The compound consists of a 1,2-benzenediamine core with two 3,4-dimethoxybenzylidene groups attached to the nitrogen atoms.

Check Digit Verification of cas no

The CAS Registry Mumber 143586-51-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,5,8 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 143586-51:
(8*1)+(7*4)+(6*3)+(5*5)+(4*8)+(3*6)+(2*5)+(1*1)=140
140 % 10 = 0
So 143586-51-0 is a valid CAS Registry Number.

143586-51-0SDS

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-(3,4-dimethoxyphenyl)-N-[2-[(3,4-dimethoxyphenyl)methylideneamino]phenyl]methanimine

1.2 Other means of identification

Product number -
Other names -

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:143586-51-0 SDS

143586-51-0Relevant articles and documents

Novel bio-essential metal based complexes linked by heterocyclic ligand: Synthesis, structural elucidation, biological investigation and docking analysis

Arun,Subramanian,Raman

, p. 67 - 76 (2016)

New series of bio-essential metal based complexes linked by Schiff base ligand (L) and 2,2′-bipyridine (bpy) have been synthesized and characterized by diverse spectral techniques such as elemental analysis, magnetic susceptibility, molar conductivity mea

Facile Synthesis of 1,2-Disubstituted Benzimidazoles Usingp-Toluenesulfonic Acid through Grinding Method

Kathing, C.,Nongkhlaw, R.,Nongrum, R.,Singh, N. G.,World Star Rani, J.

, p. 1628 - 1634 (2020/10/22)

Abstract: An efficient synthetic method for the highly selective synthesis ofpharmacologically active 1,2-disubstituted benzimidazole derivatives fromo-phenylenediamine and various aromaticaldehydes catalyzed by p-toluenesulfonic acidthrough grinding unde

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