物质信息
ID:316471
名称和标识
别名
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传统名
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
IUPAC标准名
4,4,5,5-tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolane
化合物性质
产品相关信息
其他组分
phenothiazine as stabilizer
Empirical Formula (Hill Notation)
C9H17BO2
纯度
95%
安全信息
GHS危险声明
H226-H315-H317-H319-H335
MSDS下载
个人保护装置
Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
易燃气体类别1
易燃气溶胶，第1,2类
易燃液体，类别1,2,3
自反应物质和混合物，类型B，C，D，E，F
自燃液体类别1
自燃固体类别1
自我放热物质和混合物，类别1,2
与水接触的物质和混合物，放出易燃气体类别1,2,3
有机过氧化物，类别B，C，D，E，F
GHS警示词
Warning
欧盟危险性物质标志
刺激性 (Xi)保存温度
2-8°C
GHS警示性声明
P261-P280-P305+P351+P338
危险公开号
10-36/37/38-43
RID/ADR
UN 1993 3/PG 3
联合国危险货物包装类别(PG)
3
联合国危险货物等级
3
联合国危险货物编号
1993
安全公开号
26-36/37
德国WGK号
3
理化性质
闪点
42 °C
107.6 °F
折射率
n20/D 1.4320
沸点
47-49 °C/9 mbar
密度
0.894 g/mL at 25 °C
描述信息
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
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
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