Trifluoroacetophenone

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
InChIKeyKZJRKRQSDZGHEC-UHFFFAOYSA-N
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 T
HazardClass 3
PackingGroup III
HS Code 29147090
MSDS Information
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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 apoptos is in cerebellar granule neurons.
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.
Trifluoroacetophenone Preparation Products And Raw materials
Preparation Products2,2,2-TRIFLUORO-1-PHENYL-ETHYLAMINE-->(R)-(-)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL-->PHENYL TRIFLUOROACETATE-->(S)-(+)-ALPHA-(TRIFLUOROMETHYL)BENZYL ALCOHOL-->(R)-(+)-1-PHENYL-1-PROPANOL-->3,3,3-trifluoro-2-phenyl-propanoic acid-->4-METHOXY-3-BUTEN-2-ONE-->Ethyl L(-)-lactate-->Benzenemethanol, α-(nitromethyl)-α-(trifluoromethyl)-
CARBONATE IONOPHORE III CARBONATE IONOPHORE II 4-(TRIFLUOROMETHYL)-A,A,A-TRIFLUOROACETOPHENONE,4-(TRIFLUOROMETHYL)-ALPHA,ALPHA,ALPHA-TRIFLUOROACETOPHENONE 4'-Bromoacetophenone 4'-METHOXY-2,2,2-TRIFLUOROACETOPHENONE,P-METHOXY-A,A,A-TRIFLUOROACETOPHENONE 3-Aminoacetophenone Trifluoroacetophenone 3-Nitroacetophenone 4-Nitroacetophenone 3'-Fluoroacetophenone Acetophenone 2',4'-Dichloroacetophenone 2-Bromoacetophenone 4-Fluoroacetophenone 4'-Hydroxyacetophenone 4'-METHYL-2,2,2-TRIFLUOROACETOPHENONE 4'-(Trifluoromethyl)acetophenone P-DECYL-A,A,A-TRIFLUOROACETOPHENONE

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