Substance
ID:343630
Names and Identifiers
IUPAC name
[1-(benzenesulfonyl)-1H-indol-2-yl]boronic acid
IUPAC Traditional name
1-(benzenesulfonyl)indol-2-ylboronic acid
Synonyms
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
Properties
Product Information
Linear Formula
C6H5SO2NC8H5B(OH)2
Safety Information
MSDS Link
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Physical Property
Melting Point
125-130 °C(lit.)
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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