432032
3-(Trifluoromethyl)phenylboronic acid
≥95%
Synonym(s):
3-(Trifluoromethyl)benzeneboronic acid, a,a,a-Trifluoro-m-tolueneboronic acid
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About This Item
Linear Formula:
CF3C6H4B(OH)2
CAS Number:
Molecular Weight:
189.93
Beilstein:
6084746
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.06
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Quality Level
Assay
≥95%
mp
163-166 °C (lit.)
functional group
fluoro
SMILES string
OB(O)c1cccc(c1)C(F)(F)F
InChI
1S/C7H6BF3O2/c9-7(10,11)5-2-1-3-6(4-5)8(12)13/h1-4,12-13H
InChI key
WOAORAPRPVIATR-UHFFFAOYSA-N
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Application
Reactant involved in:
- Suzuki-Miyaura cross-coupling reactions
- Aerobic oxidative cross-coupling
- Microwave-assisted Petasis reactions
- Rhodium-catalyzed addition reactions
- Syntehsis of biologically active molecules
Other Notes
Contains varying amounts of anhydride
Storage Class Code
11 - 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
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Anna Minkkilä et al.
Journal of medicinal chemistry, 51(22), 7057-7060 (2008-11-06)
A series of commercial phenyl-, heteroaryl-, alkyl-, and alkenylboronic acids were evaluated for their FAAH and MGL inhibitory activities. The compounds were generally selective for FAAH, with IC50 in the nanomolar or low-micromolar range. Eight of these compounds inhibited MGL
Gözde Murat Saltan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 188, 372-381 (2017-08-02)
In an approach to develop efficient organic optoelectronic devices to be used in light-driven systems, a series of three thiophene linked benzimidazole conjugates were synthesized and characterized. The combination of two thiophene rings to a benzimidazole core decorated with different
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