Isopropenylboronic Acid Pinacol Ester CAS 126726-62-3 Purity >99.0% (GC) Factory High Quality

Short Description:

Chemical Name: Isopropenylboronic Acid Pinacol Ester

CAS: 126726-62-3

Purity: >99.0% (GC)

Appearance: Colorless to Pale Yellow Liquid

High Quality, Commercial Production

E-Mail: alvin@ruifuchem.com


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Description:

Manufacturer Supply With High Quality, Commercial Production 
Chemical Name: Isopropenylboronic Acid Pinacol Ester 
CAS: 126726-62-3

Chemical Properties:

Chemical Name Isopropenylboronic Acid Pinacol Ester
Synonyms 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane; 2-(1-Methylethenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number 126726-62-3
CAT Number RF-PI1395
Stock Status In Stock, Production Scale Up to Tons
Molecular Formula C9H17BO2
Molecular Weight 168.04
Brand Ruifu Chemical

Specifications:

Item Specifications
Appearance Colorless to Pale Yellow Liquid
Purity / Analysis Method >99.0% (GC)
Moisture (K.F) ≤0.50%
Total Impurities <1.00%
Test Standard Enterprise Standard
Usage Pharmaceutical Intermediates

Package & Storage:

Package: Bottle, 25kg/Barrel, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.

Advantages:

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FAQ:

Application:

Isopropenylboronic Acid Pinacol Ester (CAS: 126726-62-3) 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 inhibitors. Isopropenylboronic Acid Pinacol Ester 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 Diastereoand Enantioselective allylboration of aldehydes.

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