TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC&

TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC&
  • CAS No.:871125-84-7
Other grades of this product :
TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC& Basic information
Product Name:TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC&
Synonyms:(E)-2-(3-Chlorostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;(E)-2-(3-chlorostyryl)-4,4,5,5-tetramethyl-1,3-dioxa-2-borolane;trans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester 97%;TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC;TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC&;2-[(E)-2-(3-chlorophenyl)ethenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;E-2-(3-Chlorophenyl)vinylboronic acid,pinacol ester;3-chloro-trans-beta-styrylboronic acid pinacol ester
CAS:871125-84-7
MF:C14H18BClO2
MW:264.56
EINECS:
Product Categories:
Mol File:871125-84-7.mol
TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC& Chemical Properties
Boiling point 138-140 °C0.9-1.0 mm Hg
density 1.049 g/mL at 25 °C
refractive index n20/D 1.536
Fp >230 °F
storage temp. 2-8°C
Safety Information
WGK Germany 3
HS Code 2931900090
MSDS Information
TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC& Usage And Synthesis
UsesE-2-(3-Chlorophenyl)vinylboronic acid, pinacol ester
Usestrans-2-(3-Chlorophenyl)vinylboronic acid pinacol ester can be used as a reactant:
  • To prepare aryl derivatives by C?C bond formation via palladium-catalyzed Suzuki?Miyaura reaction.
  • In the diastereoselective synthesis of alkenes via K3PO4-promoted transition metal-free nucleophilic substitution of unactivated alkyl triflates.
  • To synthesize (3-chlorophenyl)cyclopropyl boronic acid pinacol ester by reacting with diazomethane.
TRANS-2-(3-CHLOROPHENYL)VINYLBORONIC AC& Preparation Products And Raw materials

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