Grundinformationen
- Standard-SMILES
ClCCI- InChIKey
JTWWWQGSFTWWDL-UHFFFAOYSA-N- Summenformel
- C2H4ClI
- Durchschnittliche Molmasse
- 190,41 g/mol
- Monoisotopische Masse
- 189,90463
Namen und Bezeichner
- Bevorzugter Name
- 1-Chloro-2-iodoethane
- IUPAC
- 1-chloro-2-iodoethane
- Englischer Name
- 1-CHLORO-2-IODOETHANE
- Summenformel
- C2H4ClI
- Molmasse
- 190.41
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
624-70-4- PubChem CID
- 136438
- DTXSID
DTXSID60211458- EC Number
- 677-827-4
- Nikkaji
- J497I
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,9
- Polarare Oberfläche (TPSA)
- 0 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 0
- Frei drehbare Bindungen
- 1
- Schwere Atome
- 4
- Formalladung
- 0
- Komplexität
- 10
Physikochemische Eigenschaften
- Schmelzpunkt
- -15.6 °C · -15.6°C
- Siedepunkt
- 61 · 61-62°C 30mm
- Dichte
- 2 · 2,088 g/cm3
- Brechungsindex
- 1.566 · 1.5660
- Flammpunkt
- 61 · 61-62°C/30mm
- storage temp.
- 0 · 0-10°C
- Aggregatzustand
- clear liquid
- Farbe
- Colorless to Light yellow to Light orange
- Wasserlöslichkeit
- Soluble inorganic solvents. Insoluble in water.
- BRN
- 1730865 · 1730865
- CAS Datenbank
- 624 · 624-70-4(CAS DataBase Reference)
Sicherheit und Regulatorisches
Sicherheitsdaten
- ridadr
- 2810
- hs_code
- 29037800
- risk_code
- 20/21/22-68
- safety_code
- 23-36/37
- packing_group
- II
Chemie und Industrie
Anwendungen
Verwenden1-Chloro-2-iodoethane is used as a mild electrophile for iodination of metallated species, as in the conversion of an ortho-lithiated benzyl ether to the corresponding ortho-iodide. It reacts with 5-hydroxy-[1,4]naphthoquinone, and obtain the 5-(2-chloro-ethoxy)-[1,4]naphthoquinone.
Darstellung
synthetischeThe Preparative Methods of 1-chloro-2-iodoethane: prepared in 76% yield by bubbling Ethylene gas into a CH2Cl2 solution of freshly redistilled Iodine Monochloride maintained at 30 °C by ice-cooling until the temperature begins to fall. Other methods of preparation include reaction of ethylene, Copper(II) Chloride, and Iodine at 75-85 °C in a pressure reactor; reaction of excess 1,2-dichloroethane with Sodium Iodide in acetone or with Aluminum Iodide in CS2; and by reaction of 2-iodoethanol with Thionyl Chloride.
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