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CAS 72824-05-6

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4,4,5,5-Tetramethyl-2-(prop-1-enyl)-1,3,2-dioxaborolane

Description:
4,4,5,5-Tetramethyl-2-(prop-1-enyl)-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane ring structure, which features two boron atoms and a five-membered cyclic framework. This compound is typically colorless to pale yellow and is known for its stability under ambient conditions, although it may be sensitive to moisture due to the presence of boron. The presence of the prop-1-enyl group introduces reactivity, making it useful in various organic synthesis applications, particularly in the formation of carbon-carbon bonds. Its boron atoms can participate in nucleophilic reactions, making it a valuable intermediate in the synthesis of more complex molecules. Additionally, the bulky tetramethyl substituents contribute to steric hindrance, influencing its reactivity and selectivity in chemical reactions. Overall, 4,4,5,5-Tetramethyl-2-(prop-1-enyl)-1,3,2-dioxaborolane is a versatile compound in synthetic organic chemistry, particularly in the context of boron chemistry and catalysis.
Formula:C9H17BO2
Synonyms:
  • Propen-1-ylboronic acid, pinacol ester
  • Propen-1-ylboronic acid, pinacol ester 98%
  • 4,4,5,5-TetraMethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane
  • (E)-1-propenyl boronic pinacol ester
  • 1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(1-propen-1-yl)-
  • 4,4,5,5-Tetramethyl-2-(prop-1-enyl)-1,3,2-dioxaborolane
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