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
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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
signalword
Warning
Hazard Classifications
Aquatic Chronic 3 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
wgk_germany
WGK 3
flash_point_f
107.6 °F
flash_point_c
42 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Certificates of Analysis (COA)
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Articles
The synthesis of biaryl compounds via the Suzuki–Miyaura coupling reaction has become more commonplace now that many arylboronic acids are readily available.
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