N-Boc-5-methoxy-2-indolylboronic acid

• Catalog No.: 680516
• CAS Number: 290331-71-4
• M. F.: C14H18BNO5
• M. W.: 291.10742
• Purity: ≥95%

SYNONYMS

• Title: N-叔丁氧基羰基-5-甲氧基-2-吲哚硼酸
• 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-Boc-5-methoxyindole-2-boronic acid; N-(叔丁氧基羰基)-5-甲氧基吲哚-2-硼酸; 1-Boc-5-甲氧基吲哚-2-硼酸; N-(tert-Butoxycarbonyl)-5-methoxyindole-2-boronic acid

DATABASE IDS

• CAS Number: 290331-71-4
• MDL Number: MFCD04039006
• PubChem SID: 24885571

PROPERTIES

• Empirical Formula (Hill Notation): C14H18BNO5
• Purity: ≥95%
• Melting Point: 102-107 °C
• Storage Temperature: 2-8°C
• German water hazard class: 3

DETAILS

Description (English)

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

Description (简体中文)

General description
可含有不定量的酸酐。
包装
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