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CAS 629658-06-6

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2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Description:
2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is an organic compound characterized by its phenolic structure, which includes a chlorine substituent and a boron-containing moiety. The presence of the chloro group indicates potential reactivity, particularly in nucleophilic substitution reactions. The dioxaborolane group contributes to the compound's stability and solubility in organic solvents, making it useful in various synthetic applications, including cross-coupling reactions in organic synthesis. This compound may exhibit properties typical of phenols, such as acidity and the ability to form hydrogen bonds, which can influence its reactivity and interactions with other molecules. Additionally, the bulky tetramethyl substituents on the boron moiety can provide steric hindrance, affecting the compound's reactivity and selectivity in chemical reactions. Overall, 2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a versatile compound with potential applications in medicinal chemistry and materials science.
Formula:C12H16BClO3
InChI:InChI=1S/C12H16BClO3/c1-11(2)12(3,4)17-13(16-11)8-5-6-10(15)9(14)7-8/h5-7,15H,1-4H3
InChI key:InChIKey=HBKJZGOCTNRSHF-UHFFFAOYSA-N
SMILES:CC1(C)OB(OC1(C)C)C2=CC(Cl)=C(O)C=C2
Synonyms:
  • Phenol, 2-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
  • 3-Chloro-4-hydroxyphenylboronic acid pinacol ester
  • 2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
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