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CAS 1350513-18-6

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B-[(Tetrahydro-2H-pyran-4-yl)methyl]boronic acid

Description:
B-[(Tetrahydro-2H-pyran-4-yl)methyl]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. This compound features a tetrahydro-2H-pyran moiety, contributing to its structural complexity and potential reactivity. The boronic acid group imparts properties such as Lewis acidity, making it useful in various chemical reactions, including Suzuki coupling, a key reaction in organic synthesis for forming carbon-carbon bonds. Additionally, the presence of the tetrahydro-2H-pyran ring may enhance solubility and stability in certain solvents. This compound is of interest in medicinal chemistry and materials science due to its potential applications in drug development and as a building block in the synthesis of more complex molecules. Its unique structure and functional groups allow for diverse reactivity, making it a valuable compound in synthetic organic chemistry.
Formula:C6H13BO3
InChI:InChI=1S/C6H13BO3/c8-7(9)5-6-1-3-10-4-2-6/h6,8-9H,1-5H2
InChI key:InChIKey=VSONRZMBCYWOON-UHFFFAOYSA-N
SMILES:C(B(O)O)C1CCOCC1
Synonyms:
  • B-[(Tetrahydro-2H-pyran-4-yl)methyl]boronic acid
  • Boronic acid, B-[(tetrahydro-2H-pyran-4-yl)methyl]-
  • [(Oxan-4-yl)methyl]boronic acid
  • (Oxan-4-ylmethyl)boronic acid
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