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 Suppliers list

Company Name:	Yantai Sheng Kai Lun Biological Products Co. , Ltd. Gold
Tel:	13356901049
Email:	mark@sklnchem.cn

Company Name:	PharmaBlock Sciences (Nanjing),Inc.
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Email:	sales@pharmablock.com

Company Name:	Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel:	4006356688 18621169109
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trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene manufacturers

trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene Basic information

Product Name:	trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene
Synonyms:	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-;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
CAS:	83947-56-2
MF:	C14H19BO2
MW:	230.11
EINECS:
Product Categories:
Mol File:	83947-56-2.mol

trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene Chemical Properties

Melting point	27-33 °C(lit.)
Boiling point	128°C/4mm
density	0.99±0.1 g/cm3(Predicted)
refractive index	1.5290
Fp	>230 °F
storage temp.	Inert atmosphere,Store in freezer, under -20°C
form	Liquid
color	Clear colorless to pale yellow
BRN	8617179
InChI	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+
InChIKey	ARAINKADEARZLZ-ZHACJKMWSA-N
SMILES	O1C(C)(C)C(C)(C)OB1/C=C/C1=CC=CC=C1
CAS DataBase Reference	83947-56-2(CAS DataBase Reference)

Safety Information

MSDS Information

Provider	Language
SigmaAldrich	English
ALFA	English

trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene Usage And Synthesis

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

trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene Preparation Products And Raw materials

Raw materials	1-Phenylvinylboronic acid pinacol ester-->(Z)-4,4,5,5-tetramethyl-2-styryl-1,3,2-dioxaborolane-->Phenylacetylene-->Pinacolborane-->Bis(pinacolato)diboron
Preparation Products	E-Phenylethenylboronic acid-->1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-(2-phenylcyclopropyl)-

Tag:trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene(83947-56-2) Related Product Information

trans-2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)styrene trans-2-(3-Methoxyphenyl)vinylboronic acid pinacol ester, 96% Trans-2-fluorocyclohexanaMine hydrochloride BB1 cis-Stilbeneboronic acid pinacol ester E-Phenylethenylboronic acid