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2-Fluorophenylboronic acid_Molecular_structure_CAS_1993-03-9)
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2-Fluorophenylboronic acid

Catalog No. 445223 Name Sigma Aldrich
CAS Number 1993-03-9 Website http://www.sigmaaldrich.com
M. F. C6H6BFO2 Telephone 1-800-521-8956
M. W. 139.9200432 Fax
Purity Email
Storage Chembase ID: 8346

SYNONYMS

Title
2-氟苯硼酸
IUPAC name
(2-fluorophenyl)boronic acid
IUPAC Traditional name
2-fluorophenylboronic acid
Synonyms
o-fluoro-benzeneboronic acid
2-Fluorobenzeneboronic acid

DATABASE IDS

CAS Number 1993-03-9
MDL Number MFCD00674013
PubChem SID 24868168

PROPERTIES

Linear Formula FC6H4B(OH)2
Melting Point 101-110 °C(lit.)
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
German water hazard class 3

DETAILS

Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
1, 10 g in glass bottle
Application
Reactant for:
• Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes1
• Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation2
• Site-selective Suzuki-Miyaura arylation reactions3
• Rh-catalyzed enantioselective addition reactions4
• Rhodium- and Palladium-catalyzed substitution reactions5
Used for the preparation of biologically active biphenyls and arylboron difluoride Lewis acids.
Description (简体中文)
Other Notes
含不定量的酸酐
包装
1, 10 g in glass bottle
Application
Reactant for:
• Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes1
• Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation2
• Site-selective Suzuki-Miyaura arylation reactions3
• Rh-catalyzed enantioselective addition reactions4
• Rhodium- and Palladium-catalyzed substitution reactions5
用于制备具生物活性的联苯化合物和二氟化芳基硼路易斯酸。

REFERENCES