| Identification | More | [Name]
Trifluoroacetophenone | [CAS]
434-45-7 | [Synonyms]
2,2,2-TRIFLUORO-1-PHENYLETHAN-1-ONE
2,2,2-TRIFLUORO-1-PHENYLETHANONE
2,2,2-TRIFLUOROACETOPHENONE
A,A,A-TRIFLUOROACETOPHENONE
ALPHA,ALPHA,ALPHA-TRIFLUOROACETOPHENONE
PHENYL TRIFLUOROMETHYL KETONE
TRIFLUOROACETOPHENONE
TRIFLUOROACETYLBENZENE
1,1,1-Trifluoroacetophenone
2,2,2-Trifluoro-1-phenylethanoate
2,2,2-trifluoro-1-phenyl-ethanon
Acetophenone, 2,2,2-trifluoro-
Ethanone, 1,1,1-trifluoro,2-phenyl-
omega,omega,omega-Trifluoroacetophenone
Trifluoromethyl phenyl ketone
Phenyl trifluoromethyl ketone~2,2,2-Trifluoroacetophenone
alpha,alpha,alpha-Trifluoroacethophenone
Ethanone, 2,2,2-trifluoro-1-phenyl-(9CI)
Ethanone, 2,2,2-trifluoro-1-phenyl-
2,2,2-Trifluoroacetophenone 99% | [EINECS(EC#)]
207-103-1 | [Molecular Formula]
C8H5F3O | [MDL Number]
MFCD00000420 | [Molecular Weight]
174.12 | [MOL File]
434-45-7.mol |
| Safety Data | Back Directory | [Symbol(GHS) ]
 
GHS02,GHS07 | [Signal word ]
Warning | [Hazard statements ]
H226-H315-H319-H335 | [Precautionary statements ]
P210-P302+P352-P305+P351+P338 | [Hazard Codes ]
Xi,F | [Risk Statements ]
R10:Flammable.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection .
S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 1224 3/PG 3
| [WGK Germany ]
3
| [Hazard Note ]
Corrosive/Lachrymatory | [TSCA ]
T | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29147090 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Eye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
CLEAR COLORLESS TO YELLOW LIQUID | [Uses]
2,2,2-Trifluoroacetophenone is a fluorinated acetophenone with inhibitory activity of acetylcholinesterase. 2,2,2-Trifluoroacetophenone was shown to have neuroprotective activity by inhibiting apoptos
is in cerebellar granule neurons. | [General Description]
2,2,2-Trifluoroacetophenone is the starting material for the synthesis of f 3-trifluoromethyl-3-phenyldiazirine. It undergoes asymmetric reduction with optically active Grignard reagent to form 2,2,2-trifluoro-1-phenylethanol. It undergoes condensation with biphenyl, terphenyl, a mixture of biphenyl with terphenyl, phenyl ether and diphenoxybenzophenone to form new aromatic 3F polymers. | [Synthesis]
2,2,2-Trifluoroacetophenone is commonly synthesized by the following methods: (1) Trifluoroacetic acid is directly synthesized in one step by reacting directly with the Grignard reagent of bromobenzene. The yield is about 60%. The advantages of this metho |
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