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Merck

432032

Sigma-Aldrich

3-(Trifluoromethyl)phenylboronic acid

≥95%

Sinónimos:

3-(Trifluoromethyl)benzeneboronic acid, a,a,a-Trifluoro-m-tolueneboronic acid

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About This Item

Fórmula lineal:
CF3C6H4B(OH)2
Número de CAS:
Peso molecular:
189.93
Beilstein/REAXYS Number:
6084746
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.06

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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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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
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
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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