445223
2-Fluorophenylboronic acid
≥95%
Synonym(s):
2-Fluorobenzeneboronic acid, o-fluoro-benzeneboronic acid
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About This Item
Linear Formula:
FC6H4B(OH)2
CAS Number:
Molecular Weight:
139.92
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
Quality Level
Assay
≥95%
form
solid
mp
101-110 °C (lit.)
SMILES string
OB(O)c1ccccc1F
InChI
1S/C6H6BFO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4,9-10H
InChI key
QCSLIRFWJPOENV-UHFFFAOYSA-N
Related Categories
Application
Reactant for:
- Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes
- Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation
- Site-selective Suzuki-Miyaura arylation reactions
- Rh-catalyzed enantioselective addition reactions
- Rhodium- and Palladium-catalyzed substitution reactions
Used for the preparation of biologically active biphenyls and arylboron difluoride Lewis acids.
Other Notes
Contains varying amounts of anhydride
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Helvetica Chimica Acta, 78, 2026-2026 (1995)
The Journal of Organic Chemistry, 60, 3020-3020 (1995)
Mikhail Y Vorona et al.
Materials (Basel, Switzerland), 13(8) (2020-04-26)
Anthracene-based semiconductors have attracted great interest due to their molecular planarity, ambient and thermal stability, tunable frontier molecular orbitals and strong intermolecular interactions that can lead to good device field-effect transistor performance. In this study, we report the synthesis of
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