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1,4-Benzenediamine,N1,N4-bis[(4-chlorophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17866-87-4

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17866-87-4 Usage

General Description

1,4-Benzenediamine, N1, N4-bis[(4-chlorophenyl)methylene]- is a chemical compound that consists of a benzene ring with two amino groups (NH2) and two chlorine-substituted phenyl groups linked to the amino groups. It is commonly used in the production of dyes, pigments, and polymers. The compound is also used as a reagent in organic synthesis and as an intermediate in the manufacture of pharmaceuticals. However,

Check Digit Verification of cas no

The CAS Registry Mumber 17866-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,6 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 17866-87:
(7*1)+(6*7)+(5*8)+(4*6)+(3*6)+(2*8)+(1*7)=154
154 % 10 = 4
So 17866-87-4 is a valid CAS Registry Number.

17866-87-4SDS

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 1-(4-chlorophenyl)-N-[4-[(4-chlorophenyl)methylideneamino]phenyl]methanimine

1.2 Other means of identification

Product number -
Other names N.N'-Bis-(4-chlor-benzal)-p-phenylendiamin

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:17866-87-4 SDS

17866-87-4Relevant academic research and scientific papers

DBDA as a Novel Matrix for the Analyses of Small Molecules and Quantification of Fatty Acids by Negative Ion MALDI-TOF MS

Ling, Ling,Li, Ying,Wang, Sheng,Guo, Liming,Xiao, Chunsheng,Chen, Xuesi,Guo, Xinhua

, p. 704 - 710 (2018/04/14)

Matrix interference ions in low mass range has always been a concern when using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) to analyze small molecules (500 Da). In this work, a novel matrix, N1,N4-dibenzyli

Computer-aided design, synthesis, and biological studies of anticological nitrogen-containing tetraphosphonic acids against melanoma

Bekheit, Mohamed S.,Barghash, Reham F.,Abdou, Wafaa M.

, p. 1481 - 1491 (2018/07/02)

Abstract: As a part of our quest to develop new bioactive bisphosphonic acids, we synthesized a series of bis(α-aminobisphosphonic acids) in good yields (66–78%) as new entities for treating malignant melanoma. The reaction of the Schiff bases, 1,4-pheney

Novel bridgehead nitrogen bisheterocyclic systems: Synthesis, stereochemistry and antimicrobial activity of p-bis[2H, 5H-4-oxothiazol-3-yl] phenylenes and p-bis[cis-5H-3,3a-dihydropyrazolo[3,4-d]thiazol-6-yl]phenylenes

Mohan, Jag,Kumar, Ashok

, p. 631 - 634 (2007/10/03)

The facile synthesis of p-bis[cis-3,3a-dihydro-5H-pyrazolo[3,4-d]thiazol-6- yl]phenylenes 4 has been achieved by the condensation of p-bis[4-substituted phenylimine]phenylenes 1 with thioglycollic acid in toluene, using Dean-Stark water separator, to give

A facile synthesis of p-Bis(4-thiazolidinon-3-yl)phenylenes and related systems and related systems

Abdel-Megid,Awas

, p. 161 - 168 (2007/10/03)

p-Bis(4-thiazolidinon-3-yl)phenylenes were synthesized from cycloaddition of thioglycollic acid with schiff bases of p-phenylenediamine or by treatment of p-bis(thiouredo)phenylenes with ethyl chloroacetate. The effect of hydrazines, hydroxylamine, acetam

ELECTRONIC ABSORPTION SPECTRA OF AROMATIC SCHIFF BASES. PART III. p-PHENYLENEDIAMINE DERIVATIVES

Gawinecki, Ryszard,Muzalewski, Feliks

, p. 1091 - 1098 (2007/10/02)

The effect of para substituents in the benzylidene-p-dimethylaminoaniline and dibenzylidene-p-phenylenediamine molecules on their UV-VIS spectra has been studied.A linear relationship has been found between position of the most long-wavelength absorption

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