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CAS 850568-82-0

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B-[2-(2-Bromoethyl)phenyl]boronic acid

Description:
B-[2-(2-Bromoethyl)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 bromoethyl 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 bromoethyl substituent enhances its reactivity, allowing for potential applications in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method for forming carbon-carbon bonds. Additionally, the presence of the boronic acid group contributes to its solubility in polar solvents and its ability to participate in acid-base reactions. The compound's structure suggests it may also exhibit interesting biological activities, although specific biological properties would require further investigation. Overall, B-[2-(2-Bromoethyl)phenyl]boronic acid is a versatile building block in synthetic organic chemistry.
Formula:C8H10BBrO2
InChI:InChI=1S/C8H10BBrO2/c10-6-5-7-3-1-2-4-8(7)9(11)12/h1-4,11-12H,5-6H2
InChI key:InChIKey=XIPVXKZTNMWBDZ-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(CCBr)C=CC=C1
Synonyms:
  • (2-(2-Bromoethyl)phenyl)boronicacid
  • B-[2-(2-Bromoethyl)phenyl]boronic acid
  • Boronic acid, [2-(2-bromoethyl)phenyl]-
  • boronic acid, B-[2-(2-bromoethyl)phenyl]-
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