1-(苯基磺酰)-2-吲哚基硼酸

• 产品号: 563862
• CAS号: 342404-46-0
• 分子式: C14H12BNO4S
• 分子量: 301.12538

产品别名

• 标题: 1-(Phenylsulfonyl)-2-indolylboronic acid
• IUPAC标准名: [1-(benzenesulfonyl)-1H-indol-2-yl]boronic acid
• IUPAC传统名: 1-(benzenesulfonyl)indol-2-ylboronic acid
• 别名: 1-(Phenylsulfonyl)-2-indoleboronic acid; 1-(苯基磺酰)-1H-吲哚-2-基硼酸

产品登记号

• MDL号: MFCD03086094
• CAS号: 342404-46-0
• PubChem SID: 24880137

产品性质

• 线性分子式: C6H5SO2NC8H5B(OH)2
• 熔点: 125-130 °C(lit.)
• 个人保护装置: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• 德国WGK号: 3

产品详细信息

详细说明 (English)

General description
Contains varying amounts of anhydride
Packaging
1 g in glass bottle
Application
Reactant for:
• Synthesis of bioactive indolo[3,2-j]phenanthridine alkaloid, calothrixin B, via an allene-mediated electrocyclic reaction1
• Preparation of arenes via palladium and tris(tert-butyl)phosphine-catalyzed Suzuki cross-coupling2
• Structure-guided development of TbcatB inhibitors as trypanocides3
• Chemoselective and stereoselective oxidative palladium/diamine-catalyzed cross-coupling reactions4
• Petasis boronic Mannich reactions under microwave conditions5

详细说明 (简体中文)

General description
含有不定量的酸酐
包装
1 g in glass bottle
Application
Reactant for:
• Synthesis of bioactive indolo[3,2-j]phenanthridine alkaloid, calothrixin B, via an allene-mediated electrocyclic reaction1
• Preparation of arenes via palladium and tris(tert-butyl)phosphine-catalyzed Suzuki cross-coupling2
• Structure-guided development of TbcatB inhibitors as trypanocides3
• Chemoselective and stereoselective oxidative palladium/diamine-catalyzed cross-coupling reactions4
• Petasis boronic Mannich reactions under microwave conditions5