Grundinformationen
- Standard-SMILES
FCCI- InChIKey
LVYJIIRJQDEGBR-UHFFFAOYSA-N- Summenformel
- C2H4FI
- Durchschnittliche Molmasse
- 173,96 g/mol
- Monoisotopische Masse
- 173,93417635
Namen und Bezeichner
- Bevorzugter Name
- Ethane, 1-fluoro-2-iodo-
- IUPAC
- 1-fluoro-2-iodoethane
- Englischer Name
- 1-Fluoro-2-iodoethane
- Summenformel
- C2H4FI
- Molmasse
- 173.96
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
762-51-6- PubChem CID
- 69804
- DTXSID
DTXSID80227056- EC Number
- 691-351-4
- Nikkaji
- J43.003J
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,7
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 4
- Formalladung
- 0
- Komplexität
- 10
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Siedepunkt
- 98 · 98-102°C
- Dichte
- 1.9842 · 1.9842 (estimate)
- storage temp.
- -20 °C · Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Light yellow
- InChI
- InChI=1S/C2H4FI/c3-1-2-4/h1-2H2
- InChIKey
- LVYJIIRJQDEGBR-UHFFFAOYSA-N
- SMILES
- C(F)CI
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H225 (50%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 6 reports by companies from 6 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- hs_code
- 29033990
- risk_code
- 20/21/22
- hazard_code
- T
- hazard_note
- Toxic
- safety_code
- 23-36/37/39-24/25
- hazard_class
- KEEP COLD, TOXIC
Chemie und Industrie
Anwendungen
Verwenden1-Fluoro-2-iodoethane is used as a reagent in organic synthesis of several compounds including that of fluorinated U-50488 analogs for PET studies of kappa opioid receptors. It is also used in the synthesis of MK-3168, an imidazole analog which acts as a PET tracer for the imaging of brain fatty acid amide hydrolase.
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