370657
3′-(Trifluoromethoxy)acetophenone
98%
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About This Item
Linear Formula:
CF3OC6H4COCH3
CAS Number:
Molecular Weight:
204.15
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
1873998
MDL number:
SMILES string
CC(=O)c1cccc(OC(F)(F)F)c1
InChI
1S/C9H7F3O2/c1-6(13)7-3-2-4-8(5-7)14-9(10,11)12/h2-5H,1H3
InChI key
UYHTUQHYGKAYJM-UHFFFAOYSA-N
assay
98%
form
liquid
refractive index
n20/D 1.452 (lit.)
density
1.285 g/mL at 25 °C (lit.)
General description
3′-(Trifluoromethoxy)acetophenone is a meta-substituted acetophenone. Ruthenium-catalyzed reaction of carbon-hydrogen bonds in 3′-(trifluoromethoxy)acetophenone (m-(trifluoromethoxy)acetophenone) with olefins has been examined.
Application
3′-(Trifluoromethoxy)acetophenone (m-(trifluoromethoxy)acetophenone) may be used in the preparation of 4-(3′-trifluoromethoxyphenyl)-thiazol-2-yl ammonium iodide.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
181.4 °F - closed cup
flash_point_c
83 °C - closed cup
Regulatory Information
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Ruthenium-Catalyzed Addition of Carbon-Hydrogen Bonds in Aromatic Ketones to Olefins. The Effect of Various Substituents at the Aromatic Ring.
Sonoda M, et al.
Bulletin of the Chemical Society of Japan, 70(12), 3117-3128 (1997)
Michael J Gorczynski et al.
Chemistry & biology, 14(10), 1186-1197 (2007-10-27)
The two subunits of core binding factor (Runx1 and CBFbeta) play critical roles in hematopoiesis and are frequent targets of chromosomal translocations found in leukemia. The binding of the CBFbeta-smooth muscle myosin heavy chain (SMMHC) fusion protein to Runx1 is
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