426016
4,4,4-Trifluor-1-(2-furyl)-1,3-butandion
99%
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About This Item
Empirische Formel (Hill-System):
C8H5F3O3
CAS-Nummer:
Molekulargewicht:
206.12
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
99%
Form
liquid
Brechungsindex
n20/D 1.528 (lit.)
bp
203 °C (lit.)
mp (Schmelzpunkt)
19-21 °C (lit.)
Dichte
1.391 g/mL at 25 °C (lit.)
Funktionelle Gruppe
fluoro
ketone
Lagertemp.
2-8°C
SMILES String
FC(F)(F)C(=O)CC(=O)c1ccco1
InChI
1S/C8H5F3O3/c9-8(10,11)7(13)4-5(12)6-2-1-3-14-6/h1-3H,4H2
InChIKey
OWLPCALGCHDBCN-UHFFFAOYSA-N
Allgemeine Beschreibung
4,4,4-Trifluoro-1-(2-furyl)-1,3-butanedione (furoyltrifluoroacetone, FTFA) is a β-diketone. Its cytotoxic activity against human cultured tumor and normal cells has been evaluated. Reports suggest that 4,4,4-trifluoro-1-(2-furyl)-1,3-butanedione partially inhibits the oxidation of ferrocyanide in ETP (electron transport particles) isolated from beef heart mitochondria. Its reaction with N,N,N′,N′-tetramethylalkyl diamines to form ionic adducts has been investigated. The conformational analysis of the enol and keto form of FTFA has been reported.
Anwendung
Used in the efficient syntheses of perfluoroalkyl substituted azoles.
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
188.6 °F - closed cup
Flammpunkt (°C)
87 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Topography of the cristae membrane as elucidated by a new inhibitor, trifluorofurylbutanedione.
H J Harmon et al.
Biochemical and biophysical research communications, 55(1), 169-173 (1973-11-01)
Synthesis and biological evaluation of new 2-arylcarbonyl-3-trifluoromethylquinoxaline 1,4-di-N-oxide derivatives and their reduced analogues.
Solano B, et al.
Journal of Medicinal Chemistry, 50(22), 5485-5492 (2007)
Adoración Marin et al.
Experimental parasitology, 118(1), 25-31 (2007-07-07)
Derivatives of 3-trifluoromethyl-2-arylcarbonylquinoxaline 1,4-di-N-oxide (4b-g, 5b-g, 6a-g) were synthesized and evaluated for their capacity to inhibit the growth of chloroquine-resistant Plasmodium falciparum FCB1 strain in culture. Compound 7-chloro-2-(2-furylcarbonyl)-3-trifluoromethyl-1,4-quinoxaline di-N-oxide (5g) was the most active being almost 5 times more active
Acyclic tertiary diamines and 1, 4, 7,10-tetraazacyclododecane with fluorine-containing β-diketones: Leading to low melting ionic adducts.
Gupta OD, et al.
Journal of Fluorine Chemistry, 126(8), 1222-1229 (2005)
Kensuke Nakano et al.
Anticancer research, 24(2B), 711-717 (2004-05-27)
A variety of beta-diketones were evaluated for their cytotoxic profiles against oral human normal and tumor cells. Among 22 compounds (BD1-22) tested, the cytotoxicity of 3-formylchromone (BD17) (CC50=7.8 microg/mL) against human oral squamous cell carcinoma (HSC-2) cells was higher than
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