乙烯基硼酸频哪醇酯

• 产品号: 633348
• CAS号: 75927-49-0
• 分子式: C8H15BO2
• 分子量: 154.0145
• 纯 度: 95%

产品别名

• 标题: Vinylboronic acid pinacol ester
• IUPAC标准名: 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• IUPAC传统名: 2-ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
• 别名: 2-乙烯基-4,4,5,5-四甲基-1,3,2-二氧杂环戊硼烷; 2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane; 2-Vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaoborolane; 4,4,5,5-Tetramethyl-2-vinyl-1,3,2-dioxaborolane

产品登记号

• MDL号: MFCD00192492
• PubChem SID: 24882546
• CAS号: 75927-49-0

产品性质

• 其他组分: phenothiazine as stabilizer
• Empirical Formula (Hill Notation): C8H15BO2
• 纯度: 95%
• 密度: 0.908 g/mL at 25 °C(lit.)
• 闪点: 34 °C
• 闪点: 93.2 °F
• 折射率: n20/D 1.4300(lit.)
• GHS警示词: Warning
• GHS危险声明: H226-H317
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 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警示性声明: P280
• RID/ADR: UN 3272 3/PG 3
• 危险公开号: 10-43
• 安全公开号: 36/37
• 保存温度: -20°C
• 联合国危险货物等级: 3
• 联合国危险货物编号: 3272
• 联合国危险货物包装类别(PG): 3
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Packaging
1, 10 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura coupling reactions1
• Mizoroki-Heck reactions (cascade reaction)1
• Intramolecular Nozaki-Hiyama-Kishi reactions2
• Stereoselective Cu-catalyzed γ-selective and stereospecific coupling3
• Control of stereoselectivity and mechanistic portrait on intramolecular (4+1)-cycloaddition of dialkoxycarbenes4
• Regio- and stereoselective synthesis of trisubstituted alkenes via gold(I)-catalyzed hydrophosphoryloxylation of haloalkynes followed by Pd-catalyzed consecutive cross-coupling reactions5
• Asymmetric Birch reductive alkylation6Reagent used in Preparation of
• Molecular tubes for lipid sensing7
• Enzymatic inhibitors, antibiotics, receptor analogs, and other biologically significant compounds (including total syntheses)8,9,10,2

详细说明 (简体中文)

包装
1, 10 g in glass bottle
Application
Reagent used for
• Suzuki-Miyaura coupling reactions1
• Mizoroki-Heck reactions (cascade reaction)1
• Intramolecular Nozaki-Hiyama-Kishi reactions2
• Stereoselective Cu-catalyzed γ-selective and stereospecific coupling3
• Control of stereoselectivity and mechanistic portrait on intramolecular (4+1)-cycloaddition of dialkoxycarbenes4
• Regio- and stereoselective synthesis of trisubstituted alkenes via gold(I)-catalyzed hydrophosphoryloxylation of haloalkynes followed by Pd-catalyzed consecutive cross-coupling reactions5
• Asymmetric Birch reductive alkylation6Reagent used in Preparation of
• Molecular tubes for lipid sensing7
• Enzymatic inhibitors, antibiotics, receptor analogs, and other biologically significant compounds (including total syntheses)8,9,10,2