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Benzenethiol, 2-[[(4-methylphenyl)methylene]amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

159022-10-3

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159022-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159022-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,0,2 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 159022-10:
(8*1)+(7*5)+(6*9)+(5*0)+(4*2)+(3*2)+(2*1)+(1*0)=113
113 % 10 = 3
So 159022-10-3 is a valid CAS Registry Number.

159022-10-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[(4-methylphenyl)methylideneamino]benzenethiol

1.2 Other means of identification

Product number -
Other names Benzenethiol,2-[[(4-methylphenyl)methylene]amino]

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:159022-10-3 SDS

159022-10-3Relevant academic research and scientific papers

An efficient and environmental benign synthesis of 2-benzimidazoles and 2-benzothiazoles using CeCl3-NaI as catalyst

Zhu, Xun,Wei, Yunyang

, p. 119 - 121 (2013/04/23)

A one-pot condensation of an aldehyde with 1,2-phenylenediamine or 2-aminothiophenol in dimethyl carbonate at 100°C under O2 in the presence of catalytic amounts of CeCl3-NaI gave an imine intermediate, which cyclised and dehydrogenated to give 2-arylbenzimidazoles or 2-arylbenzothiazoles in good yields.

Facile preparation of 2-substituted benzoxazoles and benzothiazoles via aerobic oxidation of phenolic and thiophenolic imines catalyzed by polymer-incarcerated platinum nanoclusters

Yoo, Woo-Jin,Yuan, Hao,Miyamura, Hiroyuki,Kobayashi, Shu

supporting information; experimental part, p. 3085 - 3089 (2012/01/02)

Platinum nanoclusters supported on a polymer/carbon black composite material was found to be an excellent catalyst for the oxidative cyclization of phenolic and thiophenolic Schiff bases to 2-substituted benzoxazoles and benzothiazoles under ambient conditions. Copyright

Synthesis and Characterization of Biologically Active Organosilicon(IV) Complexes with Schiff Bases Derived from o-aminothiophenol

Singh, Kiran,Kumar, Yogender,Pundir, Ram Kumar

experimental part, p. 836 - 842 (2011/02/28)

The synthesis and structural features of some organosilicon(IV) complexes with Schiff bases derived by condensing Substituted benzaldehyde with o-aminothiophenol have been discussed. The newly synthesized compounds have been characterized by elemental ana

Structural and spectral studies of some coordination complexes of Ni(II) with N-benzylidene-2-mercaptoaniline derivatives

Ide,Ancin,?zta?,Tüzün

, p. 1 - 9 (2007/10/03)

Nickel(II) complexes of N-(4-bromobenzylidene)-2-mercaptoaniline, N-(4-methyl benzylidene)-2-mercaptoaniline and N-(4-methoxybenzylidene)-2-mercaptoaniline were prepared and investigated. The proposed structures for these complexes derived from the two-di

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