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CAS 128376-65-8

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4-(5,5-Dimethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

Description:
4-(5,5-Dimethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde, with the CAS number 128376-65-8, is an organic compound that features a benzaldehyde moiety substituted with a dioxaborolane group. This compound typically exhibits characteristics common to both aromatic aldehydes and boron-containing compounds. The presence of the aldehyde functional group suggests it is reactive, particularly in nucleophilic addition reactions, and can participate in various organic transformations. The dioxaborolane ring contributes to its stability and may enhance its reactivity in cross-coupling reactions, making it useful in synthetic organic chemistry. Additionally, the dimethyl substitution on the dioxaborolane ring can influence its steric and electronic properties, potentially affecting its solubility and reactivity. This compound may also exhibit interesting photophysical properties due to the conjugation between the aromatic system and the dioxaborolane, which can be leveraged in materials science and organic electronics. Overall, 4-(5,5-Dimethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde is a versatile building block in organic synthesis and materials development.
Formula:C12H15BO3
InChI:InChI=1/C12H15BO3/c1-12(2)8-15-13(16-9-12)11-5-3-10(7-14)4-6-11/h3-7H,8-9H2,1-2H3
SMILES:CC1(C)COB(c2ccc(cc2)C=O)OC1
Synonyms:
  • Akos Brn-0004
  • 4-(5,5-Dimethyl-1,3,2-Dioxaborinan-2-Yl)Benzaldehyde
  • 4-Formylphenylboronic Acid, Neopentyl Glycol Cyclic Ester
  • 4-Formylbenzeneboronic Acid 2,2-Dimethylpropanediol-1,3 Cyclic Ester
  • 2-(4-Formylphenyl)-5,5-Dimethyl-1,3,2-Dioxaborane
  • 4-(5,5-Dimethyl-1,3,2-dioxaborin-2-yl)benzaldehyde
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