2-Formyl-4,5-methylenedioxyphenylboronic acid

• Catalog No.: 717622
• CAS Number: 94838-88-7
• M. F.: C8H7BO5
• M. W.: 193.94918
• Purity: ≥95%

SYNONYMS

• Title: (2-甲酰基-4,5-亚甲二氧基)苯基硼酸
• IUPAC name: (6-formyl-2H-1,3-benzodioxol-5-yl)boronic acid
• IUPAC Traditional name: 6-formyl-2H-1,3-benzodioxol-5-ylboronic acid

DATABASE IDS

• CAS Number: 94838-88-7
• MDL Number: MFCD01319005

PROPERTIES

• Empirical Formula (Hill Notation): C8H7BO5
• Purity: ≥95%
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 2

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes1
• Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation2
• Synthesis of oxazoline-substituted potassium organotrifluoroborates3
• Preparation of aristolactam analogs as an antitumor agent4
• Suzuki-Miyaura coupling reactions5
• Suzuki and Negishi cross-coupling reactions6

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective preparation of indenamines by cationic palladium complex-catalyzed tandem annulation with alkynes1
• Stereoselective preparation of indenol derivatives via cationic palladium complex-catalyzed diastereoselective tandem annulation2
• Synthesis of oxazoline-substituted potassium organotrifluoroborates3
• Preparation of aristolactam analogs as an antitumor agent4
• Suzuki-Miyaura coupling reactions5
• Suzuki and Negishi cross-coupling reactions6