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CAS 2121514-36-9

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

Description:
B-[3-Bromo-5-(1-pyrrolidinylcarbonyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a bromine atom and a pyrrolidinylcarbonyl substituent on a phenyl ring, contributing to its unique reactivity and potential biological activity. The boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the presence of the pyrrolidinyl group may enhance its solubility and interaction with biological targets, suggesting potential applications in drug development. The compound's structure indicates it may exhibit specific physicochemical properties such as solubility in polar solvents and stability under certain conditions. Overall, B-[3-Bromo-5-(1-pyrrolidinylcarbonyl)phenyl]boronic acid represents a versatile building block in synthetic chemistry and pharmaceutical research.
Formula:C11H13BBrNO3
InChI:InChI=1S/C11H13BBrNO3/c13-10-6-8(5-9(7-10)12(16)17)11(15)14-3-1-2-4-14/h5-7,16-17H,1-4H2
InChI key:InChIKey=OIGGTNHRKDMFMQ-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(B(O)O)=CC(Br)=C1)N2CCCC2
Synonyms:
  • B-[3-Bromo-5-(1-pyrrolidinylcarbonyl)phenyl]boronic acid
  • Boronic acid, B-[3-bromo-5-(1-pyrrolidinylcarbonyl)phenyl]-
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