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CAS 957066-13-6

:

1,3,2-Dioxaborolane, 2-[2-(bromomethyl)-4-(trifluoromethoxy)phenyl]-4,4,5,5-tetramethyl-

Description:
1,3,2-Dioxaborolane, 2-[2-(bromomethyl)-4-(trifluoromethoxy)phenyl]-4,4,5,5-tetramethyl- is a boron-containing heterocyclic compound characterized by its dioxaborolane ring structure, which features a five-membered cyclic arrangement containing two oxygen atoms and a boron atom. This compound exhibits unique reactivity due to the presence of the boron atom, which can participate in various chemical transformations, including nucleophilic substitutions and cross-coupling reactions. The presence of the bromomethyl and trifluoromethoxy substituents on the phenyl ring enhances its potential for further functionalization and applications in organic synthesis. Additionally, the tetramethyl groups contribute to the compound's steric bulk, influencing its solubility and reactivity. This compound may be of interest in materials science and medicinal chemistry, particularly in the development of boron-based reagents or intermediates for pharmaceuticals. As with many boron-containing compounds, it is essential to handle it with care, considering potential reactivity and safety protocols.
Formula:C14H17BBrF3O3
InChI:InChI=1S/C14H17BBrF3O3/c1-12(2)13(3,4)22-15(21-12)11-6-5-10(7-9(11)8-16)20-14(17,18)19/h5-7H,8H2,1-4H3
InChI key:InChIKey=CJXUOEJTOXQAMB-UHFFFAOYSA-N
SMILES:C(Br)C1=C(C=CC(OC(F)(F)F)=C1)B2OC(C)(C)C(C)(C)O2
Synonyms:
  • 2-[2-(Bromomethyl)-4-(trifluoromethoxy)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
  • 2-Bromomethyl-4-trifluoromethoxyphenylboronic acid pinacol ester
  • 1,3,2-Dioxaborolane, 2-[2-(bromomethyl)-4-(trifluoromethoxy)phenyl]-4,4,5,5-tetramethyl-
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