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CAS 126688-98-0

:

2-[(1E)-5-Chloro-1-penten-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Description:
2-[(1E)-5-Chloro-1-penten-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound characterized by its unique dioxaborolane structure, which features a boron atom bonded to two oxygen atoms and a carbon chain. This compound contains a chloroalkene substituent, contributing to its reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions. The presence of the tetramethyl groups enhances its steric hindrance, which can influence its reactivity and solubility in various solvents. The dioxaborolane moiety is known for its ability to form stable complexes with nucleophiles, making it useful in the formation of carbon-carbon bonds. Additionally, the compound's structure suggests potential applications in medicinal chemistry and materials science, where boron-containing compounds are often explored for their unique properties. Overall, this compound exemplifies the versatility of organoboron chemistry in synthetic applications.
Formula:C11H20BClO2
InChI:InChI=1S/C11H20BClO2/c1-10(2)11(3,4)15-12(14-10)8-6-5-7-9-13/h6,8H,5,7,9H2,1-4H3/b8-6+
InChI key:InChIKey=FYHBHADHHWPOFL-SOFGYWHQSA-N
SMILES:C(=C/CCCCl)\B1OC(C)(C)C(C)(C)O1
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(5-chloro-1-pentenyl)-4,4,5,5-tetramethyl-, (E)-
  • 1,3,2-Dioxaborolane, 2-[(1E)-5-chloro-1-penten-1-yl]-4,4,5,5-tetramethyl-
  • 2-[(1E)-5-Chloro-1-penten-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • (trans-5-Chloro-1-penten-1-yl)boronic acid pinacol ester
  • 1,3,2-Dioxaborolane, 2-[(1E)-5-chloro-1-pentenyl]-4,4,5,5-tetramethyl-
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