663212
Isopropenylboronic acid pinacol ester
contains phenothiazine as stabilizer, 95%
Synonym(s):
2-Isopropenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4,4,5,5-Tetramethyl-2-(isopropenyl)-1,3,2-dioxaborolane, 4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane, 4,4,5,5-tetramethyl-2-(1-methylethenyl)-1,3,2-dioxaborolane
About This Item
Recommended Products
Quality Level
Assay
95%
contains
phenothiazine as stabilizer
refractive index
n20/D 1.4320
bp
47-49 °C/9 mbar
density
0.894 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
CC(=C)B1OC(C)(C)C(C)(C)O1
InChI
1S/C9H17BO2/c1-7(2)10-11-8(3,4)9(5,6)12-10/h1H2,2-6H3
InChI key
SVSUYEJKNSMKKW-UHFFFAOYSA-N
Related Categories
Application
- 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
Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors
- Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions
- 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
Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
107.6 °F
Flash Point(C)
42 °C
Personal Protective Equipment
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Articles
The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service