Substance
ID:321627
Names and Identifiers
IUPAC name
(6-formyl-2H-1,3-benzodioxol-5-yl)boronic acid
IUPAC Traditional name
6-formyl-2H-1,3-benzodioxol-5-ylboronic acid
Synonyms
2-Formyl-4,5-methylenedioxyphenylboronic acid(2-甲酰基-4,5-亚甲二氧基)苯基硼酸
Properties
Safety Information
Risk Statements
36/37/38
German water hazard class
2
Safety Statements
26-36
GHS Hazard statements
H315-H319-H335
European Hazard Symbols
Irritant (Xi)GHS Pictograms
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
GHS Signal Word
Warning
MSDS Link
GHS Precautionary statements
P261-P305+P351+P338
Product Information
Empirical Formula (Hill Notation)
C8H7BO5
Purity
≥95%
Molecule Details
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
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
Molecular Spectra
No Data Available
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References
No Data Available
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