441643
3-Fluorophenylboronic acid
≥95.0%
Synonym(s):
(3-Fluorophenyl-1-yl)boronic acid, 3-Fluorobenzeneboronic acid, m-Fluorophenylboronic acid, m-fluoro-Benzeneboronic acid
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All Photos(2)
About This Item
Linear Formula:
FC6H4B(OH)2
CAS Number:
Molecular Weight:
139.92
Beilstein:
3030632
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥95.0%
mp
214-218 °C (lit.)
functional group
fluoro
SMILES string
OB(O)c1cccc(F)c1
InChI
1S/C6H6BFO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4,9-10H
InChI key
KNXQDJCZSVHEIW-UHFFFAOYSA-N
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Related Categories
Application
Recently used to make novel liquid crystalline fluorobiphenylcyclohexenes and difluoroterphenyls by palladium-catalyzed cross-couplings also used in the synthesis of o-phenylphenols as potent leukotriene B4 receptor agonists.
Other Notes
Contains varying amounts of anhydride
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Customers Also Viewed
Liq. Cryst., 18, 1-1 (1995)
o-phenylphenols: potent and orally active leukotriene B4 receptor antagonists.
M J Sofia et al.
Journal of medicinal chemistry, 36(24), 3978-3981 (1993-11-26)
Journal of Materials Chemistry, 5, 2239-2239 (1995)
Chihiro Takei et al.
Chemical & pharmaceutical bulletin, 66(4), 368-374 (2018-04-03)
Previous studies have shown that reversible chemical bond formation between phenylboronic acid (PBA) and 1,3-diol can be utilized as the driving force for the preparation of layer-by-layer (LbL) films. The LbL films composed of a PBA-appended polymer and poly(vinyl alcohol)
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