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2(3H)-Thiazolethione, 4-phenyl-3-[(triphenylphosphoranylidene)amino]is a chemical compound characterized by the molecular formula C20H16N2PS. It is a thiazole derivative that features a phosphoranylideneamino group, which contributes to its unique chemical properties. 2(3H)-Thiazolethione, 4-phenyl-3-[(triphenylphosphoranylidene)amino]is of interest in the fields of chemical and medicinal research due to its potential applications in pharmaceutical research and as an intermediate in organic synthesis.

132834-48-1

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132834-48-1 Usage

Uses

Used in Pharmaceutical Research:
2(3H)-Thiazolethione, 4-phenyl-3-[(triphenylphosphoranylidene)amino]is utilized as a pharmaceutical research compound for its potential to contribute to the development of new drugs. Its unique structure and properties make it a valuable candidate for exploring novel therapeutic agents.
Used in Organic Synthesis as an Intermediate:
In the field of organic synthesis, 2(3H)-Thiazolethione, 4-phenyl-3-[(triphenylphosphoranylidene)amino]serves as an intermediate. Its reactivity and structural features allow it to be incorporated into more complex molecules, facilitating the synthesis of a variety of organic compounds for various applications.
Used in Chemical Research:
2(3H)-Thiazolethione, 4-phenyl-3-[(triphenylphosphoranylidene)amino]is also employed in chemical research to study its properties and potential reactions. Understanding its behavior in different chemical environments can lead to the discovery of new reactions and the development of innovative synthetic routes.

Check Digit Verification of cas no

The CAS Registry Mumber 132834-48-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,8,3 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 132834-48:
(8*1)+(7*3)+(6*2)+(5*8)+(4*3)+(3*4)+(2*4)+(1*8)=121
121 % 10 = 1
So 132834-48-1 is a valid CAS Registry Number.

132834-48-1SDS

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 4-phenyl-3-[(triphenyl-λ<sup>5</sup>-phosphanylidene)amino]-1,3-thiazole-2-thione

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

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More Details:132834-48-1 SDS

132834-48-1Relevant academic research and scientific papers

Aza Wittig-type reaction between the iminophosphorane derived from 3-amino-4-phenylthiazole-2(3H)-thione and iso(thio)cyanates: Preparation of mesoionic thiazolo[2,3-b]-1,3,4-thiadiazoles and N,N-bisheteroarylamines

Molina,Arques,Alias

, p. 1285 - 1298 (1992)

Aza Wittig-type reaction of iminophosphorane 1 derived from 3-amino-4-phenylthiazole-2(3H)-thione with several types of iso(thio)cyanates has been studied. The reaction of 1 with aromatic iso(thio)cyanates leads to thiazolo[2,3-b]-1,3,4-thiadiazoles 2 whi

Synthesis and electrochemical properties of the unknown N,N-bisheteroaryl amines bearing a fused heterocycle as N-substituent

Molina, Pedro,Arques, Antonio,Alias, Asuncion,Velasco, Maria D.

, p. 6219 - 6222 (2007/12/18)

The first preparation of N,N-bisheteroaryl amines bearing a fused heterocycle as N-substituent, from the iminophosphorane derived from 3-amino-4-phenylthiazoline-2(3H)-thione by sequential treatment with alkyl isocyanates and tetrafluoroboric acid is described. Its electrochemical behaviour shows that these compounds can act as organic electron transfer agents in indirect electrolysis.

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