4-Fluoroacetophenone

4-Fluoroacetophenone Basic information
Product Name:4-Fluoroacetophenone
Synonyms:Acetophenone, 4'-fluoro-;para-Fluoroacetophenone;4-FLUOROCETOPHENONE;4-FLUOROACETOPHENONE;AKOS BBS-00003234;Fluoroacetophenone color less liq;Fluoroacetophenone3;4'-Fluoroacetophenone 1-(4-Fluorophenyl)ethan-1-one 1-(4-Fluorophenyl)ethanone
CAS:403-42-9
MF:C8H7FO
MW:138.14
EINECS:206-960-9
Product Categories:Adehydes, Acetals & Ketones;Fluorine Compounds;C7 to C8;Carbonyl Compounds;Ketones;Acetophenone series;Benzenes;Aromatic Acetophenones & Derivatives (substituted);Organics;ketone;Fluorobenzene;bc0001;403-42-9
Mol File:403-42-9.mol
4-Fluoroacetophenone Structure
4-Fluoroacetophenone Chemical Properties
Melting point 4 °C
Boiling point 77-78 °C10 mm Hg(lit.)
density 1.143 g/mL at 20 °C(lit.)
refractive index n20/D 1.511(lit.)
Fp 160 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform, Ethyl Acetate
form Liquid
Specific Gravity1.138
color Clear colorless to slightly yellow
BRN 386013
InChIKeyZDPAWHACYDRYIW-UHFFFAOYSA-N
CAS DataBase Reference403-42-9(CAS DataBase Reference)
NIST Chemistry ReferenceEthanone, 1-(4-fluorophenyl)-(403-42-9)
EPA Substance Registry System4'-Fluoroacetophenone (403-42-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-23
WGK Germany 3
TSCA T
HazardClass IRRITANT
HS Code 29147090
MSDS Information
ProviderLanguage
1-(4-Fluorophenyl)ethanone English
SigmaAldrich English
ACROS English
ALFA English
4-Fluoroacetophenone Usage And Synthesis
Chemical PropertiesClear colorless to slightly yellow liquid
Uses4’-Fluoroacetophenone is an intermediate used for the synthetic preparation of various pharmaceutical good and agricultural products.
Uses4’Fluoroacetophenone is an intermediate used for the synthetic preparation of various pharmaceutical good and agricultural products.
Uses4-Fluoroacetophenone can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.
SynthesisSynthesis_403-42-9
General procedure: Oximes (1.0 mmol), Amberlyst-15 (0.02 g), FPA53-NO2(0.02 g), and solvent (1.5 mL) were introduced into a 25-cm-high, 90-mL autoclave with a glass tube inside equipped with magnetic stirrer (Scheme 2). Then the autoclave was charged with oxygen to 0.1 MPa. The reaction mixture was stirred at desirable temperature for special time. Progress of the reaction was monitored by thin-layer chromatography (TLC) or gas chromatography (GC). After the reaction, the resin (Amberlyst-15 and FPA53-NO2) was separated from the reaction mixture by filtration and extracted with 3 mL CH3CN (2 1.5 ml). The solvent was removed under reduced pressure. The residue was further purified by column chromatography on silica gel (300 mesh) with hexane/ethyl acetate to give the corresponding carbonyl compounds.
4-Fluoroacetophenone Preparation Products And Raw materials
Preparation Products4-(4-FLUORO-PHENYL)-PYRIMIDINE-2-THIOL-->4-FLUOROBENZOYLACETONITRILE-->5-(4-FLUOROPHENYL)-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE-->ETHYL 2-AMINO-4-(4-FLUOROPHENYL)THIOPHENE-3-CARBOXYLATE-->4'-PIPERAZINOACETOPHENONE-->2-Bromo-4'-fluoroacetophenone-->3-(4-FLUOROPHENYL)-1H-PYRAZOLE-4-CARBALDEHYDE-->4-Fluorophenylacetylene-->4'-Phenoxyacetophenone-->1-(4-FLUOROPHENYL)ETHYLAMINE-->ALPHA,ALPHA-DIBROMO-4-FLUOROACETOPHENONE-->2-(4-FLUOROBENZOYL)-1-BENZOFURAN-5-CARBALDEHYDE-->2-(4-FLUOROPHENYL)-1H-INDOLE-3-CARBALDEHYDE-->6-(4-FLUOROPHENYL)INDOLE-->5-(4-FLUOROPHENYL)THIOPHENE-2-CARBOXYLI&-->1-(4-Fluorophenyl)-3-(2-thienyl)-2-propen-1-one/alpha-(2-Thienylidene)-4-fluoroacetophenone-->2-(4-FLUOROPHENYL)QUINOLINE
2-Amino-2',4'-difluoroacetophenone 3',4'-Difluoroacetophenone 2-BROMO-3'-FLUOROACETOPHENONE Bis(4-fluorophenyl)-methanone 2-Chloro-4'-fluorobenzophenone 2',3',4',5'-TETRAFLUOROACETOPHENONE 2-(2-ETHOXYNAPHTHYLIDENE)-4'-FLUOROACETOPHENONE Trifluoroacetophenone 2,2,2,4'-TETRAFLUOROACETOPHENONE 4-Fluoro-4'-hydroxybenzophenone 2-(4-FLUOROBENZOYL)BENZOIC ACID 2-AMINO-3'-FLUOROACETOPHENONE HYDROCHLORIDE L-PICEIN 2-Bromoacetophenone α-(1H-1,2,4-Triazole-1-yl)-4'-fluoroacetophenone 3',5'-dichloro-2'-fluoroacetophenone 2',3',4',5',6'-PENTAFLUOROACETOPHENONE 1-(2,6-Difluorophenyl)ethan-1-one

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