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Imidazo[5,1-b]thiazole, 3-methyl-5-phenyl- is a heterocyclic organic compound characterized by a unique structure that includes a thiazole ring fused to an imidazole ring. Imidazo[5,1-b]thiazole, 3-methyl-5-phenyl- is specifically defined by the presence of a methyl group at the 3-position and a phenyl group at the 5-position. It is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its diverse chemical properties. The compound's molecular formula is C10H8N2S, reflecting its composition of carbon, hydrogen, nitrogen, and sulfur atoms. Its molecular weight is approximately 180.25 g/mol, and it exhibits a melting point of around 70-72°C. The compound is typically synthesized through various chemical reactions and can be used as a building block in the creation of more complex molecules, highlighting its importance in the field of organic chemistry and drug development.

883-34-1

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883-34-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 883-34-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,8 and 3 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 883-34:
(5*8)+(4*8)+(3*3)+(2*3)+(1*4)=91
91 % 10 = 1
So 883-34-1 is a valid CAS Registry Number.

883-34-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-5-phenylimidazo[5,1-b]thiazole

1.2 Other means of identification

Product number -
Other names 3-methylimidazo[5,1-b]thiazole

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:883-34-1 SDS

883-34-1Relevant academic research and scientific papers

Studies on Wallach's Imidazole Synthesis

Benincori, Tiziana,Brenna, Elisabetta,Sannicolo, Franco

, p. 675 - 680 (2007/10/02)

The reaction of the N-benzylamides of N-heterocyclic carboxylic acids 3 and 6-9 with phosphorus pentachloride affords heterocondensed imidazoles 4 and 10-14 by a scheme reminiscent of Wallach's imidazole synthesis starting from N,N'-dialkyloxamides.Kinetic and labelling experiments are described which support a mechanism involving nitrile ylide species and allow a better understanding of the Wallach reaction.The limiting parameter for the formation of heteroanellated imidazoles is the electron availability of the heterocyclic ring.

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