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CAS 1001907-70-5

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B-(5-Ethyl-3-pyridinyl)boronic acid

Description:
B-(5-Ethyl-3-pyridinyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a pyridine ring that has an ethyl substituent. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the pyridine ring contributes to its aromatic character and can influence its reactivity and solubility in different solvents. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are vital in the formation of carbon-carbon bonds in organic synthesis. The compound's structure suggests potential applications in drug development and materials science, particularly in the design of sensors or catalysts. Its stability and reactivity can be affected by pH and the presence of other functional groups, making it a versatile building block in chemical synthesis.
Formula:C7H10BNO2
InChI:InChI=1S/C7H10BNO2/c1-2-6-3-7(8(10)11)5-9-4-6/h3-5,10-11H,2H2,1H3
InChI key:InChIKey=ZTBRRDJHPKCUIG-UHFFFAOYSA-N
SMILES:B(O)(O)C=1C=C(CC)C=NC1
Synonyms:
  • B-(5-Ethyl-3-pyridinyl)boronic acid
  • (5-Ethylpyridin-3-yl)boronic acid
  • Boronic acid, B-(5-ethyl-3-pyridinyl)-
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