Substance
ID:341038
Names and Identifiers
IUPAC name
(4-fluorophenyl)boronic acid
IUPAC Traditional name
4-fluorophenylboronic acid
Synonyms
4-Fluorobenzeneboronic acid(4-Fluorophenyl)boric acid4-氟苯硼酸NSC 142683对氟苯硼酸4-Fluorophenylboronic acid(4-Fluorophenyl)dihydroxyboron(p-Fluorophenyl)boric acid(4-Fluorophenyl)dihydroxyboranep-Fluorobenzylboronic acidp-Fluorophenylboronic acid
Registration numbers
MDL Number
CAS Number
Beilstein Number
PubChem SID
Properties
Safety Information
European Hazard Symbols
Harmful (Xn)GHS Precautionary statements
P261-P305+P351+P338
Risk Statements
22-36/37/38
German water hazard class
3
GHS Hazard statements
H302-H315-H319-H335
MSDS Link
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Safety Statements
26-36
GHS Signal Word
Warning
Physical Property
Melting Point
262-265 °C(lit.)
Product Information
Linear Formula
FC6H4B(OH)2
Molecule Details
Other Notes
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
25 g in poly bottle
Application
Reagent used for
• Suzuki coupling using microwave and triton B catalyst1
• Pd-catalyzed direct arylation of pyrazoles with phenylboronic acids2
• Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles3
• Cu-catalyzed Petasis reactions4
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5
• Ruthenium catalyzed direct arylation6
• Rh-catalyzed asymmetric conjugate additions7
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids8
• Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions9
Contains varying amounts of anhydride
Packaging
1, 5 g in glass bottle
25 g in poly bottle
Application
Reagent used for
• Suzuki coupling using microwave and triton B catalyst1
• Pd-catalyzed direct arylation of pyrazoles with phenylboronic acids2
• Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles3
• Cu-catalyzed Petasis reactions4
• Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence5
• Ruthenium catalyzed direct arylation6
• Rh-catalyzed asymmetric conjugate additions7
• Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids8
• Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions9
Molecular Spectra
No Data Available
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References
No Data Available
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