Substance
ID:316471
Names and Identifiers
Synonyms
2-Isopropenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane4,4,5,5-Tetramethyl-2-(isopropenyl)-1,3,2-dioxaborolane2-异丙烯基-4,4,5,5-四甲基-1,3,2-二氧杂硼烷Isopropenylboronic acid pinacol ester异丙烯基硼酸频哪醇酯4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane4,4,5,5-tetramethyl-2-(1-methylethenyl)-1,3,2-dioxaborolane
IUPAC Traditional name
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
IUPAC name
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
Properties
Product Information
Contains
phenothiazine as stabilizer
Empirical Formula (Hill Notation)
C9H17BO2
Purity
95%
Safety Information
GHS Hazard statements
H226-H315-H317-H319-H335
MSDS Link
Personal Protective Equipment
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS Signal Word
Warning
European Hazard Symbols
Irritant (Xi)Storage Temperature
2-8°C
GHS Precautionary statements
P261-P280-P305+P351+P338
Risk Statements
10-36/37/38-43
RID/ADR
UN 1993 3/PG 3
Packing Group
3
Hazard Class
3
UN Number
1993
Safety Statements
26-36/37
German water hazard class
3
Physical Property
Flash Point
42 °C
107.6 °F
Refractive Index
n20/D 1.4320
Boiling Point
47-49 °C/9 mbar
Density
0.894 g/mL at 25 °C
Molecule Details
Packaging
5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed Suzuki-Miyaura cross-coupling processes1
• Inverse-electron-demand Diels-Alder reaction2
• Simmons-Smith Cyclopropanation Reaction3
• Polyene cyclization4
• Stereoselective aldol reactions5
• Grubbs cross-metathesis reaction5
• Intramolecular Suzuki-Miyaura reaction5
• Stereoselective cross-metathesis6
• Dipolar cycloaddition7
• Iodosulfonylation8
• Asymmetric conjugate addition and intramolecular hydroacylation9 Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors10 9
Reagent used for
• Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions
• Inverse-electron-demand Diels-Alder reaction2
• Simmons-Smith Cyclopropanation Reaction3
• Polyene cyclization4
• Stereoselective aldol reactions5
• Grubbs cross-metathesis reaction5
• Intramolecular Suzuki-Miyaura reaction5
• Stereoselective cross-metathesis6
• Dipolar cycloaddition
• Iodosulfonylation8
• Asymmetric conjugate addition and intramolecular hydroacylation9 Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors
5, 25 g in glass bottle
Application
Reagent used for
• Palladium-catalyzed Suzuki-Miyaura cross-coupling processes1
• Inverse-electron-demand Diels-Alder reaction2
• Simmons-Smith Cyclopropanation Reaction3
• Polyene cyclization4
• Stereoselective aldol reactions5
• Grubbs cross-metathesis reaction5
• Intramolecular Suzuki-Miyaura reaction5
• Stereoselective cross-metathesis6
• Dipolar cycloaddition7
• Iodosulfonylation8
• Asymmetric conjugate addition and intramolecular hydroacylation9 Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors10 9
Reagent used for
• Palladium-catalyzed Suzuki-Miyaura cross-coupling reactions
• Inverse-electron-demand Diels-Alder reaction2
• Simmons-Smith Cyclopropanation Reaction3
• Polyene cyclization4
• Stereoselective aldol reactions5
• Grubbs cross-metathesis reaction5
• Intramolecular Suzuki-Miyaura reaction5
• Stereoselective cross-metathesis6
• Dipolar cycloaddition
• Iodosulfonylation8
• Asymmetric conjugate addition and intramolecular hydroacylation9 Reagent used in preparation of various therapeutic kinase and enzymatic inhibitors
Molecular Spectra
No Data Available
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References
No Data Available
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