524700
3,4,5-Trifluorophenylboronic acid
≥95%
Synonym(s):
3,4,5-Trifluorobenzeneboronic acid
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About This Item
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Assay
≥95%
form
powder
mp
290-295 °C (lit.)
SMILES string
OB(O)c1cc(F)c(F)c(F)c1
InChI
1S/C6H4BF3O2/c8-4-1-3(7(11)12)2-5(9)6(4)10/h1-2,11-12H
InChI key
UHDDEIOYXFXNNJ-UHFFFAOYSA-N
Application
Reactant involved in:
- Preparation of phenylboronic catechol esters and determination of Lewis acidity
- Synthesis of benzopyranone derivatives as GABAA receptor modulators
- Synthesis of multisubstituted olefins and conjugate dienes
- Suzuki cross-coupling reactions
- Preparation of fluorinated aromatic poly(ether-amide)s
Other Notes
Contains varying amounts of anhydride.
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Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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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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