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CAS 871333-98-1

:

B-Bicyclo[2.2.1]hept-2-en-2-ylboronic acid

Description:
B-Bicyclo[2.2.1]hept-2-en-2-ylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a bicyclic structure. This compound features a bicyclo[2.2.1]heptene framework, which consists of a seven-membered ring with two double bonds, contributing to its unique reactivity and stability. The boronic acid group is known for its ability to form reversible covalent bonds with diols, making it valuable in various applications, including organic synthesis and medicinal chemistry. The compound is typically a white to off-white solid and is soluble in polar solvents like water and alcohols, which enhances its utility in biological and chemical processes. Its reactivity can be attributed to the electron-deficient nature of the boron atom, allowing it to participate in cross-coupling reactions and serve as a key intermediate in the synthesis of complex organic molecules. Overall, B-Bicyclo[2.2.1]hept-2-en-2-ylboronic acid is a versatile compound with significant implications in synthetic organic chemistry.
Formula:C7H11BO2
InChI:InChI=1S/C7H11BO2/c9-8(10)7-4-5-1-2-6(7)3-5/h4-6,9-10H,1-3H2
InChI key:InChIKey=USTOMIGLBPEIBM-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C2CC(C1)CC2
Synonyms:
  • (Bicyclo[2.2.1]hept-2-en-2-yl)boronic acid
  • B-Bicyclo[2.2.1]hept-2-en-2-ylboronic acid
  • Bicyclo[2.2.1]hept-2-en-2-ylboronic acid
  • Boronic acid, bicyclo[2.2.1]hept-2-en-2-yl-
  • boronic acid, B-bicyclo[2.2.1]hept-2-en-2-yl-
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