Substance
ID:318446
Names and Identifiers
IUPAC name
{1-[(tert-butoxy)carbonyl]-5-methoxy-1H-indol-2-yl}boronic acid
IUPAC Traditional name
1-(tert-butoxycarbonyl)-5-methoxyindol-2-ylboronic acid
Synonyms
N-(tert-Butoxycarbonyl)-5-methoxyindole-2-boronic acid1-Boc-5-甲氧基吲哚-2-硼酸N-(叔丁氧基羰基)-5-甲氧基吲哚-2-硼酸N-叔丁氧基羰基-5-甲氧基-2-吲哚硼酸N-Boc-5-methoxyindole-2-boronic acidN-Boc-5-methoxy-2-indolylboronic acid
Properties
Safety Information
Physical Property
Melting Point
102-107 °C
Product Information
Empirical Formula (Hill Notation)
C14H18BNO5
Purity
≥95%
Molecule Details
General description
May contain varying amounts of anhydride.
Packaging
1, 10 g in glass bottle
Application
Reactant for:
• Preparation of dihalogenated pyrazoles via dipolar cycloaddition by palladium-catalyzed cross-coupling processes1
• Suzuki-Miyaura cross-coupling2
• Synthesis of the isocryptolepine alkaloid and its related skeletons using a modified Pictet-Spengler reaction3
May contain varying amounts of anhydride.
Packaging
1, 10 g in glass bottle
Application
Reactant for:
• Preparation of dihalogenated pyrazoles via dipolar cycloaddition by palladium-catalyzed cross-coupling processes1
• Suzuki-Miyaura cross-coupling2
• Synthesis of the isocryptolepine alkaloid and its related skeletons using a modified Pictet-Spengler reaction3
Molecular Spectra
No Data Available
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References
No Data Available
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