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(2E)-4-(4-chlorophenyl)-5-[(4-nitrophenyl)hydrazono]-1,3-thiazol-2(5H)-imine is a thiazole derivative featuring a thiazole ring, a hydrazone group, and nitro and chloro substituents on the phenyl rings. This yellow crystalline solid has a molecular formula of C13H8ClN5O2S and a molecular weight of 333.8 g/mol. Its unique structure and properties make it a promising candidate for pharmaceutical research and organic synthesis, with potential biological activities that warrant further investigation.

39874-94-7

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39874-94-7 Usage

Uses

Used in Pharmaceutical Research:
(2E)-4-(4-chlorophenyl)-5-[(4-nitrophenyl)hydrazono]-1,3-thiazol-2(5H)-imine is used as a research compound for exploring its potential biological activities and applications in drug development. Its unique structure and properties may contribute to the discovery of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, (2E)-4-(4-chlorophenyl)-5-[(4-nitrophenyl)hydrazono]-1,3-thiazol-2(5H)-imine serves as a key intermediate or building block for the synthesis of more complex organic molecules. Its reactivity and functional groups can be utilized in various synthetic routes to access a range of target compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 39874-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,8,7 and 4 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39874-94:
(7*3)+(6*9)+(5*8)+(4*7)+(3*4)+(2*9)+(1*4)=177
177 % 10 = 7
So 39874-94-7 is a valid CAS Registry Number.

39874-94-7SDS

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 N-[(E)-[4-(4-chlorophenyl)-2-imino-1,3-thiazol-5-ylidene]amino]-4-nitroaniline

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 -
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More Details:39874-94-7 SDS

39874-94-7Downstream Products

39874-94-7Relevant academic research and scientific papers

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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