126726-62-3 Isopropenylboronic acid pinacol ester

Min.Order / FOB Price:Get Latest Price

1 Kilogram	FOB Price: USD 1000.0000

1 Kilogram

FOB Price: USD 1000.0000

Min.Order :1 Kilogram
Purity: 99%
Payment Terms : L/C,T/T

Keywords

126726-62-3 Isopropenylboronic acid pinacol ester C9H17BO2

Quick Details

Appearance:white powder
Application:pharma
PackAge:as clients needs
ProductionCapacity:1|Metric Ton|Day
Storage:RT
Transportation:sea

Superiority:

Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:

1.Noble Metal Catalysts (Pt.Pd...)

2.Organic Phosphine Ligands (Tert-butyl-phosphine.Cyclohexyl-phosphine...)

3.OLED intermediates (Fluorene,Carbazole,Boric acid...)

4.Customs Synthesis

Our advantage:

1. Higest quality and good package

2.Fast delivery

3.Better payment term

4.Fast response to customer within 6 hours

5.Good business credit in Europe ,US ,Japan ,Korea

Anyway ,if you need any chemicals from China ,Henan Tianfu can help you

Details:

Isopropenylboronic acid pinacol ester Chemical Properties

Melting point 157-161 °C

Boiling point 47-49 °C (9 mbar)

density 0.894

refractive index 1.4320

Fp 42 °C

storage temp. 2-8°C

form Liquid

color Clear, colorless to brown

InChIKey SVSUYEJKNSMKKW-UHFFFAOYSA-N

Safety Information

Hazard Codes Xi

Risk Statements 10-36/37/38-43

Safety Statements 16-26-36/37

RIDADR UN 1993

HazardClass IRRITANT

PackingGroup Ⅲ

MSDS Information

Isopropenylboronic acid pinacol ester Usage And Synthesis

Description Isopropenylboronic acid pinacol ester is a versatile ester reagent used for palladium-catalyzed Suzuki-Miyaura cross-coupling processes, inverse-electron-demand Diels-Alder reaction, Simmons-Smith cyclopropanation reaction, polyene cyclization, stereoselective aldol reactions, Grubbs cross-metathesis reaction, intramolecular Suzuki-Miyaura reaction, Stereoselective cross-metathesis, dipolar cycloaddition, iodosulfonylation, asymmetric conjugate addition and intramolecular hydroacylation and preparation of various therapeutic kinase and enzymatic inhibitors1. It can be used as an intermediate in the synthesis of variety of cyclic and acyclic organic compounds. It is also shown that the α-Substituted Allyl/Croty of this compound can be used for highly Diastereo- and Enantioselective allylboration of aldehydes2.

Sources # lang=en&region=US

# I821825

Uses suzuki reaction

View All

Visit Store