CAS 349-76-8|3′-(Trifluoromethyl)acetophenone

Introduction:Basic information about CAS 349-76-8|3′-(Trifluoromethyl)acetophenone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name3′-(Trifluoromethyl)acetophenone
CAS Number349-76-8Molecular Weight188.146
Density1.2±0.1 g/cm3Boiling Point199.0±0.0 °C at 760 mmHg
Molecular FormulaC9H7F3OMelting Point/
MSDSChineseUSAFlash Point83.9±0.0 °C
Symbol
GHS07
Signal WordWarning

Names

Name1-[3-(trifluoromethyl)phenyl]ethanone
SynonymMore Synonyms

Chemical & Physical Properties

Density1.2±0.1 g/cm3
Boiling Point199.0±0.0 °C at 760 mmHg
Molecular FormulaC9H7F3O
Molecular Weight188.146
Flash Point83.9±0.0 °C
Exact Mass188.044907
PSA17.07000
LogP2.72
Vapour Pressure0.3±0.3 mmHg at 25°C
Index of Refraction1.447
InChIKeyABXGMGUHGLQMAW-UHFFFAOYSA-N
SMILESCC(=O)c1cccc(C(F)(F)F)c1

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective EquipmentEyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard CodesXi:Irritant
Risk PhrasesR36/37/38
Safety PhrasesS26-S36
RIDADRNONH for all modes of transport
WGK Germany1
HS Code29147090

Customs

HS Code2914700090
SummaryHS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles3

More Articles
Highly enantioselective catalytic phenylation of ketones with a constrained geometry titanium catalyst.

Org. Lett. 5(20) , 3641-4, (2003)

[reaction: see text] The catalytic asymmetric addition of phenyl groups from diphenylzinc to ketones is reported. The catalyst, generated from a dihydroxy bis(sulfonamide) ligand and titanium tetraiso...

Asymmetric transfer hydrogenation: chiral ligands and applications.

Chem. Soc. Rev. 35(3) , 226-36, (2006)

Hydrogen transfer reduction processes are attracting increasing interest from synthetic chemists in view of their operational simplicity and high selectivity. In this tutorial review the most signific...

A practical catalytic asymmetric addition of alkyl groups to ketones.

J. Am. Chem. Soc. 124(37) , 10970-1, (2002)

Many catalysts will promote the asymmetric addition of alkylzinc reagents to aldehydes. In contrast, there are no reports of additions to ketones that are both general and highly enantioselective. We ...

Synonyms

1-Acetyl-3-(trifluoromethyl)benzene
3’-(Trifluoromethyl)acetophenone
Acetophenone, 3'-(trifluoromethyl)-
m-Trifluoromethylacetophenone
1-[3-(Trifluoromethyl)phenyl]ethanone
3′-(Trifluoromethyl)acetophenone
FXFFR CV1
Ethanone, 1-[3-(trifluoromethyl)phenyl]-
EINECS 206-490-4
3'-(TrifluoroMethyl)acetophenone
3‘-(Trifluoromethyl)acetophenone
1-[3-(trifluoromethyl)phenyl]ethan-1-one
MFCD00000391
1-[3-(Trifluoromethyl)phenyl]-1-ethanone
3-Acetylbenzotrifluoride
1-(3-trifluoromethyl-phenyl)-ethanone
1-(3-(Trifluoromethyl)phenyl)ethanone
3-(Trifluoromethyl)acetophenone
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