(2-Bromo-4-methylthiazol-5-yl)methanol


Chemical Name: (2-Bromo-4-methylthiazol-5-yl)methanol
CAS Number: 933782-03-7
Product Number: AG01EE33(AGN-PC-0WCZ2O)
Synonyms:
MDL No:
Molecular Formula:
Molecular Weight:

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound (2-Bromo-4-methylthiazol-5-yl)methanol, also known as $name$, is a versatile chemical reagent commonly employed in organic synthesis. With its unique molecular structure, $name$ plays a crucial role in the development of various pharmaceuticals, agrochemicals, and other specialty chemicals.In chemical synthesis, $name$ serves as a key building block for the construction of complex molecules. Its reactive functional groups enable it to participate in a wide range of reactions, including nucleophilic substitution, palladium-catalyzed coupling, and cross-coupling reactions. By incorporating $name$ into the synthesis process, chemists can access a diverse array of molecular scaffolds and structural motifs that are essential for drug discovery and material science.Moreover, the presence of the thiazole ring in $name$ imparts unique physicochemical properties, making it an attractive candidate for developing bioactive compounds. Through strategic modifications and derivatization of $name$, researchers can introduce desired functionalities and enhance the biological activity or pharmacokinetic profiles of the resulting molecules.Overall, the use of (2-Bromo-4-methylthiazol-5-yl)methanol in chemical synthesis exemplifies its significance as a valuable tool for crafting intricate chemical structures and advancing innovation in the field of organic chemistry.