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CAS 913836-06-3

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B-[4-(2-Bromoethoxy)phenyl]boronic acid

Description:
B-[4-(2-Bromoethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a bromoethoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the bromine atom enhances its reactivity, allowing for potential cross-coupling reactions, particularly in the context of Suzuki-Miyaura coupling, which is a widely used method for forming carbon-carbon bonds. Additionally, the ethoxy group can influence solubility and reactivity, making the compound suitable for diverse chemical transformations. Its unique structure also suggests potential applications in the development of pharmaceuticals or agrochemicals, where boronic acids are often utilized for their ability to modulate biological activity. Overall, B-[4-(2-Bromoethoxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C8H10BBrO3
InChI:InChI=1/C8H10BBrO3/c10-5-6-13-8-3-1-7(2-4-8)9(11)12/h1-4,11-12H,5-6H2
InChI key:InChIKey=IJUQRBJDVKMDFJ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(OCCBr)C=C1
Synonyms:
  • B-[4-(2-Bromoethoxy)phenyl]boronic acid
  • Boronic acid, B-[4-(2-bromoethoxy)phenyl]-
  • [4-(2-Bromoethoxy)phenyl]boronic acid
  • Boronic acid, [4-(2-bromoethoxy)phenyl]-
  • (4-(2-Bromoethoxy)phenyl)boronicacid
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