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3,5-Bis(trifluoromethyl)phenylboronic acid_Molecular_structure_CAS_73852-19-4)
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3,5-Bis(trifluoromethyl)phenylboronic acid

Catalog No. 471070 Name Sigma Aldrich
CAS Number 73852-19-4 Website http://www.sigmaaldrich.com
M. F. C8H5BF6O2 Telephone 1-800-521-8956
M. W. 257.9255192 Fax
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Storage Chembase ID: 9526

SYNONYMS

Title
3,5-双(三氟甲基)苯硼酸
IUPAC name
[3,5-bis(trifluoromethyl)phenyl]boronic acid
IUPAC Traditional name
3,5-bis(trifluoromethyl)phenylboronic acid
Synonyms
3,5-Di(trifluoromethyl)benzeneboronic acid

DATABASE IDS

Beilstein Number 7379990
CAS Number 73852-19-4
PubChem SID 24870695
MDL Number MFCD00051850

PROPERTIES

Linear Formula (CF3)2C6H3B(OH)2
Melting Point 217-220 °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 (简体中文)
Other Notes
含不定量的酸酐
包装
5 g in glass bottle
Application
Reactant involved in the synthesis of:
• Methylene-arylbutenones via carbonylative arylation of allenols1
• 4-aminoquinoline analogs via Ullman / Suzuki / Negishi coupling2
• Primary amino acid derivatives with anticonvulsant activity3
• Alkyl arylcarbamates via Cu-catalyzed coupling with potassium cyanate4
• Aryl-substituted succinimides and cyclic ketones by asymmetric conjugate addition5
• Axially chiral dicarboxylic acids for asymmetric Mannich-type reactions6
Description (English)
Other Notes
Contains varying amounts of anhydride
Packaging
5 g in glass bottle
Application
Reactant involved in the synthesis of:
• Methylene-arylbutenones via carbonylative arylation of allenols1
• 4-aminoquinoline analogs via Ullman / Suzuki / Negishi coupling2
• Primary amino acid derivatives with anticonvulsant activity3
• Alkyl arylcarbamates via Cu-catalyzed coupling with potassium cyanate4
• Aryl-substituted succinimides and cyclic ketones by asymmetric conjugate addition5
• Axially chiral dicarboxylic acids for asymmetric Mannich-type reactions6

REFERENCES