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CAS 2121513-64-0

:

1,3,2-Dioxaborolane, 2-(5-chloro-2-fluoro-4-methoxyphenyl)-4,4,5,5-tetramethyl-

Description:
1,3,2-Dioxaborolane, 2-(5-chloro-2-fluoro-4-methoxyphenyl)-4,4,5,5-tetramethyl- is a boron-containing heterocyclic compound characterized by its dioxaborolane ring structure, which typically features a five-membered ring containing two oxygen atoms and one boron atom. This compound is notable for its potential applications in organic synthesis and medicinal chemistry, particularly due to the presence of the chloro, fluoro, and methoxy substituents on the phenyl ring, which can influence its reactivity and biological activity. The presence of these functional groups may enhance its lipophilicity and alter its electronic properties, making it a candidate for various chemical reactions, including cross-coupling reactions. Additionally, the tetramethyl substitution contributes to steric hindrance, which can affect the compound's stability and reactivity. Overall, this compound exemplifies the diverse chemistry of boron-containing compounds and their utility in developing new materials and pharmaceuticals.
Formula:C13H17BClFO3
InChI:InChI=1S/C13H17BClFO3/c1-12(2)13(3,4)19-14(18-12)8-6-9(15)11(17-5)7-10(8)16/h6-7H,1-5H3
InChI key:InChIKey=SSVALZQIWPKGHV-UHFFFAOYSA-N
SMILES:FC1=C(B2OC(C)(C)C(C)(C)O2)C=C(Cl)C(OC)=C1
Synonyms:
  • 1,3,2-Dioxaborolane, 2-(5-chloro-2-fluoro-4-methoxyphenyl)-4,4,5,5-tetramethyl-
  • 2-(5-Chloro-2-fluoro-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 5-Chloro-2-fluoro-4-methoxyphenylboronic acid pinacol ester
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