trans-2-(3-Fluorophenyl)vinylboronic acid

trans-2-(3-Fluorophenyl)vinylboronic acid Suppliers list

Company Name:	Chongqing Chemdad Co., Ltd
Tel:	+86-023-6139-8061 +86-86-13650506873
Email:	sales@chemdad.com
Products Intro:	Product Name:trans-2-(3-Fluorophenyl)vinylboronic acid CAS:849062-22-2 Package:1kg，2kg，5kg，10kg，25kg

Company Name:	Alchem Pharmtech,Inc.
Tel:	8485655694
Email:	sales@alchempharmtech.com
Products Intro:	CAS:849062-22-2 Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-73265

Company Name:	Wuhan Chemwish Technology Co., Ltd
Tel:	027-67849912
Email:	sales@chemwish.com
Products Intro:	Product Name:trans-2-(3-Fluorophenyl)vinylboronic acid CAS:849062-22-2 Purity:0.98 Package:1g;5g;25g;4940g

Company Name:	CONIER CHEM AND PHARMA LIMITED
Tel:	+8618523575427
Email:	sales@conier.com
Products Intro:	CAS:849062-22-2 Purity:0.99 Package:1kg

Company Name:	career henan chemical co
Tel:	+86-0371-86658258 15093356674;
Email:	factory@coreychem.com
Products Intro:	Product Name:trans-2-(3-Fluorophenyl)vinylboronic acid CAS:849062-22-2 Purity:98%min Package:1KG;2USD

trans-2-(3-Fluorophenyl)vinylboronic acid manufacturers

trans-2-(3-Fluorophenyl)vinylboronic acid Basic information

Product Name:	trans-2-(3-Fluorophenyl)vinylboronic acid
Synonyms:	trans-2-(3-Fluorophenyl)vinylboronic acid;(3-Fluorostyryl)boronic acid;(E)-2-(3-Fluorophenyl)ethenylboronic acid;Boronic acid, B-[(1E)-2-(3-fluorophenyl)ethenyl]-;(E)-(3-Fluorostyryl)boronic acid
CAS:	849062-22-2
MF:	C8H8BFO2
MW:	165.96
EINECS:
Product Categories:	blocks;BoronicAcids;Alkenyl;Boronic Acids;Boronic Acids and Derivatives;6
Mol File:	849062-22-2.mol

trans-2-(3-Fluorophenyl)vinylboronic acid Chemical Properties

Melting point	184-186 °C (lit.)
Boiling point	313.9±44.0 °C(Predicted)
density	1.228±0.06 g/cm3(Predicted)
storage temp.	under inert gas (nitrogen or Argon) at 2-8°C
pka	9.57±0.43(Predicted)

Safety Information

WGK Germany	3
HS Code	2931900090

MSDS Information

trans-2-(3-Fluorophenyl)vinylboronic acid Usage And Synthesis

Uses

Reactant for:

Enantioselective diastereoselective synthesis of tetracyclins via metal-catalyzed ring opening of meso-oxabicyclic alkenes followed by hydrogenation and Friedel-Crafts alkylation
Palladium-catalyzed Suzuki-Miyaura coupling reactions
Preparation of anticonvulsant agents
Preparation of piperazinyl pyrimidylhydroxamic acid deriatives as histone deacetylase inhibitors and antitumor agents
Preparation of ethyl-substituted conjugated dienoates and dienones by stereoselective Suzuki cross-coupling

trans-2-(3-Fluorophenyl)vinylboronic acid Preparation Products And Raw materials

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