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trans-2-Phenylvinylboronic acid pinacol ester

ALDRICH/570214

Synonym: (E)-4,4,5,5-Tetramethyl-2-(2-phenylvinyl)-1,3,2-dioxaborolane; (E)-4,4,5,5-Tetramethyl-2-styryl-1,3,2-dioxaborolane; 4,4,5,5-Tetramethyl-2-((E)-2-phenylethenyl)-1,3,2-dioxaborolane; trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene; trans-2-Styreneboronic acid pinacol ester

CAS Number: 83947-56-2
Empirical Formula (Hill Notation): C14H19BO2
Molecular Weight: 230.11
MDL Number: MFCD03453666
Linear Formula: C6H5CH=CHBO2C2(CH3)4
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-570214-1G 1 g
$70.80
1/EA
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This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 570214-1G

 

InChI 1S/C14H19BO2/c1-13(2)14(3,4)17-15(16-13)11-10-12-8-6-5-7-9-12/h5-11H,1-4H3/b11-10+
InChI key ARAINKADEARZLZ-ZHACJKMWSA-N
mp 27-33 °C (lit.)
SMILES string [H]C(B1OC(C)(C)C(C)(C)O1)=C([H])c2ccccc2
Application: 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
Packaging: 1 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
mp 27-33 °C (lit.)
UNSPSC 12352103

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