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TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE

TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE Structure
CAS No.
83947-56-2
Chemical Name:
TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE
Synonyms
(E)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane;E-Styrylboronic acid pinacol ester;BETA-STYRYLBORONIC ACID PINACOL ESTER;TRANS-STYRYLBORONIC ACID, PINACOL ESTER;trans-2-Styreneboronic acid pinacol ester;trans-2-Phenylvinylboronic acid pinacol ester;trans-^b-Styrylboronic acid pinacol ester, 99%;[(E)-2-Phenylvinyl]boronic acid, pinacol ester;trans-beta-Styrylboronic acid pinacol ester, 99%;(E)-2-Phenylethylene-1-boronic acid, pinacol ester
CBNumber:
CB3437702
Molecular Formula:
C14H19BO2
Molecular Weight:
230.11
MOL File:
83947-56-2.mol
MSDS File:
SDS
Modify Date:
2023/5/4 15:13:58

TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE Properties

Melting point 27-33 °C(lit.)
Boiling point 128°C/4mm
Density 0.99±0.1 g/cm3(Predicted)
refractive index 1.5290
Flash point >230 °F
storage temp. Inert atmosphere,Store in freezer, under -20°C
form Liquid
color Clear colorless to pale yellow
BRN 8617179
InChIKey ARAINKADEARZLZ-ZHACJKMWSA-N
CAS DataBase Reference 83947-56-2(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 570214 trans-2-Phenylvinylboronic acid pinacol ester 83947-56-2 1G ₹3550.6 2022-06-14 Buy
ALFA India ALF-L19529-MD trans-beta-Styrylboronic acid pinacol ester, 98% 83947-56-2 250mg ₹4610 2022-05-26 Buy
ALFA India ALF-L19529-03 trans-beta-Styrylboronic acid pinacol ester, 98% 83947-56-2 1g ₹4933 2022-05-26 Buy
Product number Packaging Price Buy
570214 1G ₹3550.6 Buy
ALF-L19529-MD 250mg ₹4610 Buy
ALF-L19529-03 1g ₹4933 Buy

TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE Chemical Properties,Uses,Production

Uses

Reactant for:

  • Oxidative coupling reactions catalyzed by areneruthenium
  • Cycloaddition reactions
  • Preparation of allyl vinyl ethers via Cu-catalyzed coupling with alcohols
  • Preparation of 5-vinyl-3-pyridinecarbonitriles as PKCθ inhibitors
  • Diastereoselective addition to zincated hydrazones and stereospecific trapping of boron/zinc bimetallic intermediates by carbon electrophiles
  • Regioselective and stereoselective Pd-catalyzed chelate-controlled intermolecular oxidative Heck reactions

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E-Styrylboronic acid pinacol ester BETA-STYRYLBORONIC ACID PINACOL ESTER TRANS-STYRYLBORONIC ACID, PINACOL ESTER TRANS-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)STYRENE trans-2-Phenylvinylboronic acid pinacol ester trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2- trans-2-Styreneboronic acid pinacol ester, trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene trans-^b-Styrylboronic acid pinacol ester, 99% trans-beta-Styrylboronic acid pinacol ester, 99% trans-2-Styreneboronic acid pinacol ester (E)-2-Phenylethylene-1-boronic acid, pinacol ester trans-beta-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene 1,3,2-Dioxaborolane, 4,4,5,5-tetraMethyl-2-[(1E)-2-phenylethenyl]- (E)-2-Phenylethylene-1-boronic acid, pinacol ester, trans-beta-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene, [(E)-2-Phenylethenyl]boronic acid, pinacol ester [(E)-2-Phenylvinyl]boronic acid, pinacol ester (E)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane (E)-4,4,5,5-Tetramethyl-2-(2-phenylvinyl)-1,3,2-dioxaborolane 4,4,5,5-Tetramethyl-2-((E)-2-phenylethenyl)-1,3,2-dioxaborolane 83947-56-2 C6H5CHCHBO2C2CH34 Alkenyl Boronate Esters Boronic Acids and Derivatives Organometallic Reagents