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Trifluoroacetophenone

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CAS:434-45-7
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CAS:434-45-7
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  • Trifluoroacetophenone
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  • $10.00 / 1kg
  • 2025-04-15
  • CAS:434-45-7
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: 20ton
Trifluoroacetophenone Basic information
Product Name:Trifluoroacetophenone
Synonyms:α,α,α-Trifluoroacetophenone, Phenyl trifluoromethyl ketone;1-Phenyl-2,2,2-trifluoroethanone;alpha,alpha,alpha-Trifluoroacetophenone,99%;2,2,2-Trifluoro-1-phenyl-1-ethanone;2,2,2-trifluroacetophenone;NSC 42752;A,A,A-TRIFLUOROACETOPHENONE FOR SYNTHESI;1-Phenyl-2,2,2-trifluoroethan-1-one
CAS:434-45-7
MF:C8H5F3O
MW:174.12
EINECS:207-103-1
Product Categories:Aromatic Acetophenones & Derivatives (substituted);ketone;ACETYLHALIDE
Mol File:434-45-7.mol
Trifluoroacetophenone Structure
Trifluoroacetophenone Chemical Properties
Melting point -40 °C
Boiling point 165-166 °C (lit.) 46-48 °C/14 mmHg (lit.)
density 1.24 g/mL at 25 °C (lit.)
refractive index n20/D 1.458(lit.)
Fp 107 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Ethyl Acetate
form Liquid
color Clear colorless to yellow
Specific Gravity1.240
Water Solubility PRACTICALLY INSOLUBLE
BRN 1866286
InChI1S/C8H5F3O/c9-8(10,11)7(12)6-4-2-1-3-5-6/h1-5H
InChIKeyKZJRKRQSDZGHEC-UHFFFAOYSA-N
SMILESFC(F)(F)C(=O)c1ccccc1
CAS DataBase Reference434-45-7(CAS DataBase Reference)
NIST Chemistry ReferenceEthanone, 2,2,2-trifluoro-1-phenyl-(434-45-7)
EPA Substance Registry SystemEthanone, 2,2,2-trifluoro-1-phenyl- (434-45-7)
Safety Information
Hazard Codes Xi,F
Risk Statements 10-36/37/38
Safety Statements 26-36-37/39-16
RIDADR UN 1224 3/PG 3
WGK Germany 3
Hazard Note Corrosive/Lachrymatory
TSCA TSCA listed
HazardClass 3
PackingGroup III
HS Code 29147090
Storage Class3 - Flammable liquids
Hazard ClassificationsEye Irrit. 2
Flam. Liq. 3
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
2,2,2-Trifluoroacetophenone English
ACROS English
SigmaAldrich English
ALFA English
Trifluoroacetophenone Usage And Synthesis
Chemical PropertiesCLEAR COLORLESS TO YELLOW LIQUID
Uses2,2,2-Trifluoroacetophenone is a fluorinated acetophenone with inhibitory activity of acetylcholinesterase. 2,2,2-Trifluoroacetophenone was shown to have neuroprotective activity by inhibiting apoptosis in cerebellar granule neurons.
General Description2,2,2-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.
Synthesis2,2,2-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 method are simple operation and cheap raw materials. Disadvantages: exothermic and low yield. (2) in -40 , carbon disulfide solvent, the role of Lewis acid AlCl3, trifluoroacetic anhydride and the benzene ring to pay the acylation reaction preparation, yield of about 70%. Advantages of the method: one-step synthesis. Disadvantages: solvent toxicity, AlCl3 is difficult to deal with, the use of strong acid, strong alkali corrosion equipment and pollution of the environment. (3) Trifluoromethane gas and benzoate or benzoyl chloride reaction, preparation. Yield 70-80%.
Tag:Trifluoroacetophenone(434-45-7) Related Product Information
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