Isopropenylboronic acid pinacol ester

• Catalog No.: 663212
• CAS Number: 126726-62-3
• M. F.: C9H17BO2
• M. W.: 168.04108
• Purity: 95%

SYNONYMS

• Title: 异丙烯基硼酸频哪醇酯
• IUPAC name: 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
• IUPAC Traditional name: 4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
• Synonyms: 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; 4,4,5,5-Tetramethyl-2-(isopropenyl)-1,3,2-dioxaborolane; 2-异丙烯基-4,4,5,5-四甲基-1,3,2-二氧杂硼烷; 2-Isopropenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

DATABASE IDS

• CAS Number: 126726-62-3
• MDL Number: MFCD08276843
• PubChem SID: 24884621

PROPERTIES

• Contains: phenothiazine as stabilizer
• Empirical Formula (Hill Notation): C9H17BO2
• Purity: 95%
• Boiling Point: 47-49 °C/9 mbar
• Density: 0.894 g/mL at 25 °C
• Flash Point: 42 °C
• Flash Point: 107.6 °F
• Refractive Index: n20/D 1.4320
• GHS Signal Word: Warning
• GHS Hazard statements: H226-H315-H317-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P261-P280-P305 + P351 + P338
• RID/ADR: UN 1993 3/PG 3
• Risk Statements: 10-36/37/38-43
• Safety Statements: 26-36/37
• Storage Temperature: 2-8°C
• Hazard Class: 3
• UN Number: 1993
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (English)

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

Description (简体中文)

包装
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