4-吡唑硼酸频哪醇酯

Sigma Aldrich

ID: 525057

名称和标识

IUPAC标准名

4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

IUPAC传统名

4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

别名

4,4,5,5-Tetramethyl-2-(pyrazol-4-yl)-1,3,2-dioxaborolane4,4,5,5-四甲基-2-(1H-吡唑-4-基)-1,3,2-二氧杂戊硼烷4-Pyrazoleboronic acid pinacol ester4,4,5,5-Tetramethyl-2-(1H-pyrazol-2-yl)-1,3,2-dioxaborolane4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazolePyrazol-4-ylboronic acid pinacol ester4-吡唑硼酸频哪醇酯4,4,5,5-Tetramethyl-2-(1H-pyrazol-4-yl)-1,3,2-dioxaborolane

数据登录号

CAS号

269410-08-4

MDL号

MFCD03453063

PubChem SID

24874465

化合物性质

安全信息

欧盟危险性物质标志

刺激性 (Xi)

个人保护装置

dust mask type N95 (US), Eyeshields, Gloves

危险公开号

36/37/38

GHS警示性声明

P261-P305+P351+P338

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

GHS警示词

Warning

MSDS下载

下载链接

德国WGK号

安全公开号

26-36

GHS危险声明

H315-H319-H335

理化性质

熔点

142-146 °C(lit.)

产品相关信息

线性分子式

(CH3)4C2O2BC3N2H3

纯度

97%

描述信息

包装
1, 5, 25 g in glass bottle
Legal Information
Boron Molecular 制造
Application
Reagent used for
• Suzuki-Miyaura cross-couplings1
• Ruthenium-catalyzed asymmetric hydrogenation2 Reagent used in preparation of inhibitors of many highly significant therapeutic enzymes and kinases containing the privileged scaffold pyrazole, including
• VEGF3
• Aurora3,4
• Rho (ROCK)2
• Janus Kinase 2 (JAK)5
• c-MET6
• ALK6
• S-nitrosoglutathione reductase7
• CDC78
• Acetyl-CoA carboxylase9
• Prosurvival Bcl-2 protein10
• Viral RNA-Dependent RNA polymerase11
• Long Chain Fatty Acid Elongase 612
• PI313
• AKT14
• Chk115
• Protein Kinase B16

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参考文献