Product Name:4-Methyl-2-phenylthiazole-5-carbohydrazide

IUPAC Name:4-methyl-2-phenyl-1,3-thiazole-5-carbohydrazide

CAS:61292-08-8
Molecular Formula:C11H11N3OS
Purity:97%
Catalog Number:CM522829
Molecular Weight:233.29

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CM522829-1g in stock ƻŔ
CM522829-5g in stock Ŕǯň

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Product Details

CAS NO:61292-08-8
Molecular Formula:C11H11N3OS
Melting Point:-
Smiles Code:O=C(C1=C(C)N=C(C2=CC=CC=C2)S1)NN
Density:
Catalog Number:CM522829
Molecular Weight:233.29
Boiling Point:
MDL No:MFCD00174004
Storage:

Category Infos

Thiazoles
Thiazoles are very important functional groups in medicinal chemistry. They act as ligands on a variety of biological matrices. Thiazoles are used in a wide range of therapeutic applications, such as antibacterial, antiretroviral, antifungal, antiallergic, antihypertensive, pain treatment, and to control symptoms of schizophrenia.

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Product Other Information

Product Overview 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide (MPTCH) is an organic compound which is a member of the thiazole family.
Physical Properties It is a white, crystalline solid which is soluble in water. 
Chemical Properties The main advantage of using 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide in laboratory experiments is that the synthesis process is relatively simple and can be carried out in a laboratory setting. The compound is not very stable and can degrade over time. 
Synthesis and Application It has been used as a reagent for the synthesis of other compounds, such as 2-amino-4-methyl-1,3-thiazole-5-carbohydrazide and 2-amino-3-methyl-1,3-thiazole-5-carbohydrazide. In addition, 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide has been used as a catalyst for chemical reactions, such as the reaction of 4-methyl-2-phenylthiazole with hydrazine hydrate. Finally, 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide has been used as a substrate for the study of biochemical and physiological effects.
Future Directions These include further research into the biochemical and physiological effects of the compound, as well as research into the potential therapeutic applications of 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide. In addition, further research into the synthesis process and the mechanism of action of 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide could lead to the development of more efficient and effective laboratory methods for synthesizing the compound. Finally, research into the stability of 4-Methyl-2-phenyl-1,3-thiazole-5-carbohydrazide could lead to new methods for storing and handling the compound.