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2-Acetylphenylboronic acid_Molecular_structure_CAS_308103-40-4)
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2-Acetylphenylboronic acid

Catalog No. 470805 Name Sigma Aldrich
CAS Number 308103-40-4 Website http://www.sigmaaldrich.com
M. F. C8H9BO3 Telephone 1-800-521-8956
M. W. 163.96626 Fax
Purity Email
Storage Chembase ID: 32617

SYNONYMS

Title
2-乙酰苯基硼酸
IUPAC name
(2-acetylphenyl)boronic acid
IUPAC Traditional name
2-acetylphenylboronic acid
Synonyms
2-Acetylbenzeneboronic acid

DATABASE IDS

MDL Number MFCD01321263
PubChem SID 24870684
CAS Number 308103-40-4

PROPERTIES

Linear Formula CH3COC6H4B(OH)2
Melting Point 170 °C (dec.)(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
5, 25 g in glass bottle
Application
Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions1
• Rhodium-catalyzed annulation of ynamides2
• Transient masking of hydroxy groups3
• Cationic palladium complex-catalyzed diastereoselective tandem annulation4
• Hydrogen peroxide mediated formation of heteroaryl ethers5
• Copper-catalyzed transmetalation and homocoupling6
Description (简体中文)
Other Notes
含有不定量的酸酐
包装
5, 25 g in glass bottle
Application
Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions1
• Rhodium-catalyzed annulation of ynamides2
• Transient masking of hydroxy groups3
• Cationic palladium complex-catalyzed diastereoselective tandem annulation4
• Hydrogen peroxide mediated formation of heteroaryl ethers5
• Copper-catalyzed transmetalation and homocoupling6

REFERENCES