5-吲哚硼酸

• 产品号: 666467
• CAS号: 144104-59-6
• 分子式: C8H8BNO2
• 分子量: 160.96562

产品别名

• 标题: 5-Indolylboronic acid
• IUPAC标准名: (1H-indol-5-yl)boronic acid
• IUPAC传统名: 1H-indol-5-ylboronic acid
• 别名: 5-吲哚基硼酸; 5-Indoleboronic acid; Indole-5-boronic acid; 吲哚-5-硼酸

产品登记号

• MDL号: MFCD01319013
• PubChem SID: 24884799
• CAS号: 144104-59-6

产品性质

• 线性分子式: (C8H6N)B(OH)2
• 熔点: 170-175 °C
• GHS警示词: Warning
• GHS危险声明: H315-H319-H335
• 欧盟危险性物质标志: 刺激性(Irritant) (Xi)
• 个人保护装置: dust mask type N95 (US), Eyeshields, Gloves
• GHS警示性声明: P261-P305 + P351 + P338
• 危险公开号: 36/37/38
• 安全公开号: 26
• 保存温度: 2-8°C
• 德国WGK号: 3

产品详细信息

详细说明 (English)

Application
Substrate used in a rhodium-catalyzed 1,4-addition to unprotected maleimides.7
Reactant involved in the synthesis of biologically active molecules including:
• Indole inhibitors of MMP-13 for arthritic disease treatment1
• Substituted pyrimidines acting as tubulin polymerization inhibitors2Reactant involved in Suzuki coupling reactions for synthesis of
• Aryl- hetarylfurocoumarins3
• Aryl-substituted oxabenzindoles and methanobenzindoles4Reactant involved in:
• Oxidative cross-coupling with mercaptoacetylenes5
• Trifluoromethylation6
General description
May contain varying amounts of anhydride
Packaging
1 g in glass bottle

详细说明 (简体中文)

Application
用于未保护马来酰亚胺的铑催化 1,4-加成反应的基质。7
Reactant involved in the synthesis of biologically active molecules including:
• Indole inhibitors of MMP-13 for arthritic disease treatment1
• Substituted pyrimidines acting as tubulin polymerization inhibitors2Reactant involved in Suzuki coupling reactions for synthesis of
• Aryl- hetarylfurocoumarins3
• Aryl-substituted oxabenzindoles and methanobenzindoles4Reactant involved in:
• Oxidative cross-coupling with mercaptoacetylenes5
• Trifluoromethylation6
General description
可能含有不定量的酸酐
包装
1 g in glass bottle