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CAS 134892-21-0

:

2-[(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]cyclopentanone

Description:
2-[(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]cyclopentanone, with CAS number 134892-21-0, is an organic compound characterized by the presence of a cyclopentanone moiety and a dioxaborolane group. The dioxaborolane structure contributes to its potential reactivity, particularly in organoboron chemistry, where it can participate in various reactions such as cross-coupling and nucleophilic substitutions. The compound is likely to exhibit moderate polarity due to the presence of both hydrophobic cyclopentanone and polar boron-containing groups. Its molecular structure suggests potential applications in synthetic organic chemistry, especially in the development of boron-based reagents or intermediates. Additionally, the presence of bulky tetramethyl groups may influence its steric properties, affecting its reactivity and interactions with other molecules. Overall, this compound represents a unique combination of functional groups that may be valuable in various chemical synthesis applications.
Formula:C12H21BO3
InChI:InChI=1S/C12H21BO3/c1-11(2)12(3,4)16-13(15-11)8-9-6-5-7-10(9)14/h9H,5-8H2,1-4H3
InChI key:InChIKey=RDHUDWTZJNHYMH-UHFFFAOYSA-N
SMILES:C(B1OC(C)(C)C(C)(C)O1)C2C(=O)CCC2
Synonyms:
  • 2-[(Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]cyclopentan-1-one
  • 2-[(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]cyclopentan-1-one
  • 1,3,2-Dioxaborolane, cyclopentanone deriv.
  • Cyclopentanone, 2-[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]-
  • 2-[(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]cyclopentanone
  • (3-oxocyclopentyl)boronic acid pinacol ester
  • 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclopentanone
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