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112143-03-0

Phenol, 4,4'-[1,4-phenylenebis[(E)-nitrilomethylidyne]]bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 112143-03-0 Structure

  • Basic information

    1. Product Name: Phenol, 4,4'-[1,4-phenylenebis[(E)-nitrilomethylidyne]]bis-
    2. Synonyms: bis-(4-hydroxy-benzylidene)-p-phenylenediamine;Bis-(4-hydroxy-benzyliden)-p-phenylendiamin;4,4'-[1,4-phenylenebis(nitrilomethylidyne)]bis-phenol;
    3. CAS NO:112143-03-0
    4. Molecular Formula: C20H16N2O2
    5. Molecular Weight: 316.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112143-03-0.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: Phenol, 4,4'-[1,4-phenylenebis[(E)-nitrilomethylidyne]]bis-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phenol, 4,4'-[1,4-phenylenebis[(E)-nitrilomethylidyne]]bis-(112143-03-0)
    11. EPA Substance Registry System: Phenol, 4,4'-[1,4-phenylenebis[(E)-nitrilomethylidyne]]bis-(112143-03-0)

  • 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: 112143-03-0(Hazardous Substances Data)

112143-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112143-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,4 and 3 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 112143-03:
(8*1)+(7*1)+(6*2)+(5*1)+(4*4)+(3*3)+(2*0)+(1*3)=60
60 % 10 = 0
So 112143-03-0 is a valid CAS Registry Number.

112143-03-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis-(4-hydroxybenzylidene)benzene-1,4-diamine

1.2 Other means of identification

Product number -
Other names Bis-(4-hydroxy-benzyliden)-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:112143-03-0 SDS

112143-03-0Relevant articles and documents

Stannous chloride catalyzed synthesis of Schiff bases from hydroxybenzaldehydes and determination of their antioxidant activity by ABTS and DPPH assay

Bora, Gyanashree,Gogoi, Dipankoj,Saikia, Subhasmita,Pareek, Archana,Handique, Jyotirekha G

, (2019)

Abstract: Phenolic compounds play a very important role in human life because of their antioxidant activity which can prevent harmful diseases caused by free radicals. In the present work, we have synthesized some Schiff bases by the reaction of different

N,N′-bisbenzylidenebenzene-1,4-diamines and N,N′- bisbenzylidenenaphthalene-1,4-diamines as sirtuin type 2 (SIRT2) inhibitors

Kiviranta, P?ivi H.,Lepp?nen, Jukka,Kyrylenko, Sergiy,Salo, Heikki S.,Lahtela-Kakkonen, Maija,Tervo, Anu J.,Wittekindt, Carsten,Suuronen, Tiina,Kuusisto, Erkki,J?rvinen, Tomi,Salminen, Antero,Poso, Antti,Wallén, Erik A. A.

, p. 7907 - 7911 (2007/10/03)

A series of N,N′-bisbenzylidenebenzene-1,4-diamine and N,N′-bisbenzylidenenaphthalene-1,4-diamine derivatives were synthesized as inhibitors for human sirtuin type 2 (SIRT2). The design of the new compounds was based on two earlier reported hits from molecular modeling and virtual screening. The most potent compound was N,N′-bis(2-hydroxybenzylidene) benzene-1,4-diamine, which was equipotent with the most potent hit compound and well-known SIRT2 inhibitor sirtinol.

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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