251194
1-Fluorpentan
98%
Synonym(e):
Amylfluorid
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Alle Fotos(1)
About This Item
Lineare Formel:
CH3(CH2)4F
CAS-Nummer:
Molekulargewicht:
90.14
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
98%
Form
liquid
Brechungsindex
n20/D 1.36 (lit.)
bp
62-63 °C (lit.)
Dichte
0.789 g/mL at 25 °C (lit.)
Funktionelle Gruppe
alkyl halide
fluoro
SMILES String
CCCCCF
InChI
1S/C5H11F/c1-2-3-4-5-6/h2-5H2,1H3
InChIKey
OEPRBXUJOQLYID-UHFFFAOYSA-N
Allgemeine Beschreibung
Dual luminescence of 4-N,N-dimethylaminobenzonitrile has been observed in 1-fluoropentane.
Anwendung
1-Fluoropentane has been used in the synthesis of 6-F-B10H13 and 6-Cl- B10H13 (halodecaboranes).
Zubehör
Produkt-Nr.
Beschreibung
Preisangaben
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
-9.4 °F - closed cup
Flammpunkt (°C)
-23 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Faceshields, Gloves
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The role of the solvent in the dual luminescence of 4-N, N-dimethylaminobenzonitrile.
Suppan P.
Chemical Physics Letters, 128(2), 160-161 (1986)
C F Nhachi et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(8), 705-713 (1988-08-01)
Phenobarbitone pretreatment potentiated hepatocyte lesions in male rats 24 hr after treatment with 1-fluoropentane (3.5 mg/kg body weight) and 1-fluorohexane (0.17 mg/kg body weight). Serum levels of the enzymes ornithine carbamyltransferase, glutamic-pyruvic transaminase and gamma-glutamyltranspeptidase were significantly elevated by the
William C Ewing et al.
Inorganic chemistry, 47(19), 8580-8582 (2008-08-30)
The high-yield syntheses of 6-X-B 10H 13 [X = Cl (88%), Br (96%), I (84%)] resulted from the cage-opening reactions of the (NH 4 (+)) 2B 10H 10 (2-) salt with ionic-liquid-based superacidic hydrogen halides, while both the previously unknown
K R Harikumar et al.
Nature chemistry, 1(9), 716-721 (2010-12-03)
The controlled imprinting of surfaces with specified patterns is important in the development of nanoscale devices. Previously, such patterns were created using self-assembled physisorbed adsorbate molecules that can be stabilized on the surface by subsequent chemical bonding. Here we show
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