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480425-34-1

3-Bromo-2-butoxyphenylboronic acid

Catalog#: AR00DAGB  |   CAS#: 480425-34-1  |   MDL#: MFCD04974101  |   MF: C10H14BBrO3  |   MW: 272.9314

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Catalog Number AR00DAGB
Chemical Name 3-Bromo-2-butoxyphenylboronic acid
CAS Number 480425-34-1
Molecular Formula C10H14BBrO3
Molecular Weight 272.9314
MDL Number MFCD04974101
SMILES CCCCOc1c(Br)cccc1B(O)O

3-Bromo-2-butoxyphenyl)boronic acid is a versatile compound widely utilized in chemical synthesis. Its unique structure makes it a valuable building block in organic chemistry, particularly in the field of pharmaceutical development. This boronic acid derivative serves as a crucial intermediate in the synthesis of various biologically active molecules and pharmaceutical drugs.One of the key applications of (3-Bromo-2-butoxyphenyl)boronic acid is in the formation of carbon-carbon and carbon-heteroatom bonds through the Suzuki-Miyaura coupling reaction. This reaction, catalyzed by a palladium catalyst, allows for the efficient creation of complex molecular structures. By incorporating this boronic acid derivative into the reaction, chemists can selectively introduce the phenylboronic acid moiety into target molecules, enabling precise control over the structure and functionality of the final product.Furthermore, (3-Bromo-2-butoxyphenyl)boronic acid can participate in other cross-coupling reactions, such as the Chan-Lam coupling, Stille coupling, and Heck reaction, expanding its utility in synthetic chemistry. These versatile transformations enable the incorporation of the phenylboronic acid group into a diverse range of organic molecules, facilitating access to new compounds with potent biological activities.Overall, the strategic incorporation of (3-Bromo-2-butoxyphenyl)boronic acid in chemical synthesis offers chemists a powerful tool for the construction of complex molecular architectures, making it a valuable reagent in the development of novel pharmaceuticals, agrochemicals, and materials.
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