(2,5-dibromo-1,3-thiazol-4-yl)methanol


Chemical Name: (2,5-dibromo-1,3-thiazol-4-yl)methanol
CAS Number: 934236-32-5
Product Number: AG00GRUH(AGN-PC-00Z4XJ)
Synonyms:
MDL No:
Molecular Formula: C4H3Br2NOS
Molecular Weight: 272.94572

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



The compound (2,5-Dibromothiazol-4-yl)methanol, also known as $name$, is a versatile reagent widely utilized in chemical synthesis due to its unique properties. One primary application of this compound is in the synthesis of various heterocyclic compounds. By incorporating (2,5-Dibromothiazol-4-yl)methanol into a reaction, chemists can introduce the thiazole moiety into target molecules, adding complexity and diversity to the final products. This compound acts as a valuable building block in the construction of pharmaceuticals, agrochemicals, and materials with desirable properties. Its ability to undergo various chemical transformations, such as nucleophilic substitutions and cross-coupling reactions, makes it a valuable tool for synthetic chemists aiming to access structurally diverse molecules with potential biological activities. Furthermore, the presence of bromine atoms enhances the reactivity and selectivity of (2,5-Dibromothiazol-4-yl)methanol, allowing for precise control over the synthetic pathways. In summary, the application of (2,5-Dibromothiazol-4-yl)methanol in chemical synthesis enables the efficient construction of complex molecules with tailored structures and functionalities.