物质信息
ID:343630
名称和标识
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 acid1-(苯基磺酰)-1H-吲哚-2-基硼酸1-(Phenylsulfonyl)-2-indolylboronic acid1-(苯基磺酰)-2-吲哚基硼酸
化合物性质
产品相关信息
线性分子式
C6H5SO2NC8H5B(OH)2
安全信息
理化性质
熔点
125-130 °C(lit.)
描述信息
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
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
分子图谱
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参考文献
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