Product Name:(5E)-5-(5-Chloro-2-methoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one

IUPAC Name:(5E)-5-[(5-chloro-2-methoxyphenyl)methylidene]-2-sulfanyl-4,5-dihydro-1,3-thiazol-4-one

CAS:352700-55-1
Molecular Formula:C11H8ClNO2S2
Purity:95%
Catalog Number:CM518785
Molecular Weight:285.76

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CM518785-5g in stock ƥȐƥ

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Product Details

CAS NO:352700-55-1
Molecular Formula:C11H8ClNO2S2
Melting Point:-
Smiles Code:O=C1N=C(S)S/C1=C/C2=CC(Cl)=CC=C2OC
Density:
Catalog Number:CM518785
Molecular Weight:285.76
Boiling Point:
MDL No:MFCD04968969
Storage:Sealed in dry,2-8°C.

Category Infos

Thiazolines
Thiazolines are a group of isomeric five-membered heterocyclic compounds containing both sulfur and nitrogen. Thiazoline exists in three isomeric forms namely 2-thiazoline, 3-thiazoline and 4-thiazoline. Oxazolines, oxazoles, thiazolines, and thiazoles form the characteristic heterocyclic building blocks of lissoclinum peptide alkaloids.

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Product Other Information

Product Overview (5E)-5-(5-Chloro-2-methoxybenzylidene)-2-mercapto-1,3-thiazol-4(5H)-one, or 5-CMST for short, is a compound of interest in the scientific research community due to its unique properties and potential applications. It is a member of the thiazole family of compounds and has a wide range of potential applications, including in drug discovery, drug synthesis, and other biomedical and pharmaceutical research.
Synthesis and Application 5-CMST can be synthesized using a variety of methods, including the Hantzsch reaction and the Grignard reaction. The Hantzsch reaction involves the formation of an aryl-thiazole from aryl aldehydes and thiourea, and is the most commonly used method for the synthesis of 5-CMST. The Grignard reaction is another method for the synthesis of 5-CMST, and involves the addition of a Grignard reagent to an aldehyde or ketone. 5-CMST has a wide range of potential applications in scientific research, including in drug discovery, drug synthesis, and other biomedical and pharmaceutical research. It has been used in the synthesis of several drugs, including anticoagulants, anti-inflammatory drugs, and anti-cancer drugs. It has also been used in the synthesis of novel compounds with potential therapeutic applications. In addition, 5-CMST has been used in the synthesis of fluorescent probes and in the study of enzyme-catalyzed reactions.
Future Directions There are a number of potential future directions for the use of 5-CMST in scientific research. These include further investigation of its biochemical and physiological effects, as well as its potential therapeutic applications. In addition, further research could be conducted on the compound’s mechanism of action and its potential for use in drug synthesis and drug discovery. Finally, 5-CMST could be used in the study of enzyme-catalyzed reactions and in the synthesis of novel compounds with potential therapeutic applications.