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2-Thiazolamine, 5-[(4-nitrophenyl)azo]-4-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

59775-83-6

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59775-83-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59775-83-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,7 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59775-83:
(7*5)+(6*9)+(5*7)+(4*7)+(3*5)+(2*8)+(1*3)=186
186 % 10 = 6
So 59775-83-6 is a valid CAS Registry Number.

59775-83-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2-imino-4-phenyl-1,3-thiazol-5-ylidene)amino]-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 5-[2-(4-nitrophenyl)diazen-1-yl]-4-phenyl-1,3-thiazol-2-amine

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:59775-83-6 SDS

59775-83-6Downstream Products

59775-83-6Relevant academic research and scientific papers

Potential COVID-19 Drug Candidates Based on Diazinyl-Thiazol-Imine Moieties: Synthesis and Greener Pastures Biological Study

Abu-Melha, Sraa,Al-Kaff, Nadia S.,Edrees, Mastoura Mohamed,Gomha, Sobhi M.,Riyadh, Sayed M.,Said, Musa A.

, (2022/01/24)

A novel series of 1-aryl-N-[4-phenyl-5-(arylazo)thiazol-2-yl)methanimines has been synthesized via the condensation of 2-amino-4-phenyl-5-arylazothiazole with various aromatic aldehydes. The synthesized imines were characterized by spectroscopic technique

HETEROCYCLIC AZO DYE HYBRID MATERIAL, MANUFACTURING METHOD THEREOF AND FABRIC PRODUCTION

-

, (2018/04/14)

This invention discloses a heterocyclic azo dye hybrid material. The manufacturing method of the heterocyclic azo dye hybrid material includes: providing a 2-aminothiazole intermediate performing a coupling reaction with the 2-aminothiazole intermediate and a p-nitroaniline to obtain a thiadiazole azo dye performing a reaction with the thiadiazole azo dye and a vinyltriethoxysilane to obtain a precursor and performing a condensation reaction with the precursor and a vanadium pentoxide to obtain the heterocyclic azo dye hybrid material.

Sol-gel synthesis of organic-inorganic hybrid materials comprising boehmite, silica, and thiazole dye

Yen, Ming-Shien,Kuo, Mu-Cheng

experimental part, p. 349 - 354 (2012/05/19)

A hybrid material was prepared from a boehmite sol and a thiazole derived azo dye. The thiazole azo dyes were subjected to hydrolytic polycondensation with vinyltriethoxysilane, tetraethoxysilane, and aluminium isopropoxide in different ratios to afford a

The synthesis of vinyltriethoxysilane-modified heteroaryl thiazole dyes and silica hybrid materials

Yen, Ming-Shien,Chen, Chien-Wen

experimental part, p. 129 - 132 (2010/11/04)

Hybrid materials composed of tetraethoxysilane and heteroaryl 4-substituent-2-aminothiazoles were prepared. 4-Substituted acetophenone, thiourea and iodide were used to generate the intermediate, 4-substituted-2-aminothiazole, as coupling component, which was then coupled with p-nitroaniline and p-methoxyaniline to yield heteroaryl 4-substitued thiazole azo dyes. The dyes subsequently underwent hydrolytic polycondensation with vinyltriethoxysilane and tetraethoxysilane to yield hybrid, heteroaryl thiazole azo dyes, whose chemical structure was characterized using FT-IR, 29Si NMR, 1H NMR and EDS.

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