126726-62-3 Isopropenylboronic acid pinacol ester CAS NO.126726-62-3

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Min.Order: 1 Kilogram
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Available Specifications:
pharma(0-1)Metric Ton1000/Metric Ton0USD

Product Details

Keywords

126726-62-3
Isopropenylboronic acid pinacol ester
C9H17BO2

Quick Details

ProName: 126726-62-3 Isopropenylboronic acid pi...
CasNo: 126726-62-3
Molecular Formula: C9H17BO2
Appearance: white powder
Application: pharma
DeliveryTime: prompt
PackAge: as clients needs
Port: Shanghai,QingdaoTianjin,Guangzhou
ProductionCapacity: 1 Metric Ton/Day
Purity: 99%
Storage: RT
Transportation: sea
LimitNum: 1 Kilogram
Moisture Content: N/A
Impurity: N/A
N/A: N/A

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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