CymitQuimica logo

CAS 1256355-16-4

:

B-[3-Bromo-5-(1-pyrrolidinyl)phenyl]boronic acid

Description:
B-[3-Bromo-5-(1-pyrrolidinyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a bromine atom and a pyrrolidine ring attached to a phenyl group, contributing to its unique reactivity and potential biological activity. The presence of the bromine substituent enhances its electrophilic character, while the pyrrolidine moiety may impart specific steric and electronic properties that can influence its interactions in biological systems. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as a building block for more complex molecules. Its solubility and stability can vary depending on the solvent and conditions, and it is important to handle it with care due to the potential reactivity of the boronic acid group.
Formula:C10H13BBrNO2
InChI:InChI=1S/C10H13BBrNO2/c12-9-5-8(11(14)15)6-10(7-9)13-3-1-2-4-13/h5-7,14-15H,1-4H2
InChI key:InChIKey=IDBGWBMXFPQRRD-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(C=C(Br)C1)N2CCCC2
Synonyms:
  • Boronic acid, B-[3-bromo-5-(1-pyrrolidinyl)phenyl]-
  • 3-Bromo-5-pyrrolidinophenylboronic acid
  • 3-Bromo-5-(pyrrolidin-1-yl)phenylboronic acid
  • [3-Bromo-5-(pyrrolidin-1-yl)phenyl]boronic acid
  • B-[3-Bromo-5-(1-pyrrolidinyl)phenyl]boronic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.