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CAS 153737-25-8

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3,3-DIETHOXY-1-PROPENYLBORONIC ACID PINACOL ESTER

Description:
3,3-Diethoxy-1-propenylboronic acid pinacol ester is an organoboron compound characterized by the presence of a boron atom bonded to a propenyl group and two ethoxy groups. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds through cross-coupling reactions. The pinacol ester functionality enhances its stability and solubility in organic solvents. Additionally, the presence of the propenyl group allows for further functionalization, making it a versatile intermediate in synthetic chemistry. The compound is generally handled with care due to the reactivity of boron species, and it may be sensitive to moisture and air. Its applications can extend to medicinal chemistry, materials science, and the development of boron-containing ligands in catalysis. Overall, 3,3-Diethoxy-1-propenylboronic acid pinacol ester is a valuable compound in the toolkit of synthetic chemists.
Formula:C13H25BO4
InChI:InChI=1/C13H25BO4/c1-7-15-11(16-8-2)9-10-14-17-12(3,4)13(5,6)18-14/h9-11H,7-8H2,1-6H3/b10-9+
Synonyms:
  • 3,3-Diethoxy-1-Propenylboronic Acid Pinacol Ester, (E)+(Z)
  • 3,3-Diethoxy-1-Propenylboronic Acid Picanol Ester, (E)+(Z)
  • 3,3-Diethoxy-trans-1-propenylboronic acid pinacol ester, 97%
  • 2-[(1E)-3,3-diethoxyprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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