7(4H)-Benzothiazolone, 2-bromo-5,6-dihydro-5,5-dimethyl-


Chemical Name: 7(4H)-Benzothiazolone, 2-bromo-5,6-dihydro-5,5-dimethyl-
CAS Number: 10513-26-5
Product Number: AG0093KA(AGN-PC-0H2BM8)
Synonyms:
MDL No:
Molecular Formula: C9H10BrNOS
Molecular Weight: 260.1508

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2-Bromo-5,5-dimethyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional properties. This compound serves as a valuable building block in the development of various organic molecules due to its ability to undergo diverse chemical transformations.One of the notable applications of 2-Bromo-5,5-dimethyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one in chemical synthesis is its role as a precursor for the synthesis of heterocyclic compounds. By introducing this compound into a reaction, chemists can access a broad array of novel heterocycles with potentially valuable biological or pharmaceutical activities. Additionally, the bromo substituent on the molecule can serve as a key functional group for further derivatization, allowing for the introduction of additional functionalities or structural modifications.Furthermore, 2-Bromo-5,5-dimethyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one can also be employed in cross-coupling reactions to construct more complex molecular frameworks. Its unique structure and reactivity make it a valuable reagent for forming carbon-carbon or carbon-heteroatom bonds, enabling the synthesis of intricate organic molecules with high efficiency and selectivity.Overall, the versatility of 2-Bromo-5,5-dimethyl-5,6-dihydrobenzo[d]thiazol-7(4H)-one makes it an indispensable tool in chemical synthesis for the creation of diverse functionalized compounds and heterocyclic structures with potential applications in various fields including medicinal chemistry, materials science, and agrochemicals.