3′-(Trifluoromethyl)acetophenone

Modify Date: 2024-01-02 12:04:30

3′-(Trifluoromethyl)acetophenone Structure
3′-(Trifluoromethyl)acetophenone structure
Common Name 3′-(Trifluoromethyl)acetophenone
CAS Number 349-76-8 Molecular Weight 188.146
Density 1.2±0.1 g/cm3 Boiling Point 199.0±0.0 °C at 760 mmHg
Molecular Formula C9H7F3O Melting Point N/A
MSDS Chinese USA Flash Point 83.9±0.0 °C
Symbol GHS07
GHS07
Signal Word Warning

 Names

Name 1-[3-(trifluoromethyl)phenyl]ethanone
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 199.0±0.0 °C at 760 mmHg
Molecular Formula C9H7F3O
Molecular Weight 188.146
Flash Point 83.9±0.0 °C
Exact Mass 188.044907
PSA 17.07000
LogP 2.72
Vapour Pressure 0.3±0.3 mmHg at 25°C
Index of Refraction 1.447

 Safety Information

Symbol GHS07
GHS07
Signal Word Warning
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305 + P351 + P338
Personal Protective Equipment Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes Xi:Irritant
Risk Phrases R36/37/38
Safety Phrases S26-S36
RIDADR NONH for all modes of transport
WGK Germany 1
HS Code 29147090

 Customs

HS Code 2914700090
Summary HS: 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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