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HCID 69804Erstellt: 26. Oktober 2026

Ethane, 1-fluoro-2-iodo-

1-fluor-2-jodethan · 2-fluoroethyliodide · 1-IODO-2-FLUOROETHANE · 2-FLUORO-1-IODOETHANE · 1-fluoro-2-iodo-ethan · 1-FLUORO-2-IODOETHANE · 1-Fluoro-2-iodoethane98% · 1-Fluoro-2-iodoethane, 97+%

https://huagongshe.com/de/chemical/69804

Molekülstruktur von Ethane, 1-fluoro-2-iodo-

Identifikatoren & physikalische Daten

CAS No.762-51-6
SummenformelC2H4FI
Durchschnittliche Molmasse173,96 g/mol
Monoisotopische Masse173,93417635 g/mol
SMILESFCCI
InChIKeyLVYJIIRJQDEGBR-UHFFFAOYSA-N
PubChem CID69804
EC No.691-351-4
DTXSIDDTXSID80227056

Chemische & physikalische Eigenschaften

XLogP1,7
Polarare Oberfläche (TPSA)0
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen1
Schwere Atome4
Formalladung0
Komplexität10
SpringerMaterials PropertiesCoriolis coupling
Siedepunkt98-102°C
Dichte1.9842 (estimate)
LagerbedingungenKeep in dark place,Inert atmosphere,Store in freezer, under -20°C
Aggregatzustandclear liquid
FarbeColorless to Light yellow
InChIInChI=1S/C2H4FI/c3-1-2-4/h1-2H2
InChIKeyLVYJIIRJQDEGBR-UHFFFAOYSA-N
SMILESC(F)CI

Sicherheit & Vorschriften

GHS-EinstufungDangerH225 (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.
Hazard Classes and CategoriesFlam. Liq. 2 (50%)
Zollcode29033990
R-Sätze (R)20/21/22
GefahrensymboleT
hazard_noteToxic
Sicherheitshinweise (S)23-36/37/39-24/25
GefahrenklasseKEEP COLD, TOXIC

Anwendungen & Verwendung

Verwenden

1-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.