Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HCID 2793751Erstellt: 26. Oktober 2026

Isopropylphosphonic dichloride

AURORA KA-6763 · 2-dichlorophosphorylpropane · Isopropyl phosphonic dichloride · 1-METHYLETHYL-PHOSPHONICDICHLORIDE · P-(1-Methylethyl)phosphonic dichloride · Phosphonic dichloride, P-(1-methylethyl)- · Isopropylphosphonic dichloride, tech. 90%

https://huagongshe.com/de/chemical/2793751

Molekülstruktur von Isopropylphosphonic dichloride

Identifikatoren & physikalische Daten

CAS No.1498-46-0
SummenformelC3H7Cl2OP
Durchschnittliche Molmasse160,96 g/mol
Monoisotopische Masse159,9611572 g/mol
SMILESCC(C)P(=O)(Cl)Cl
InChIKeyKLHAQQISVPLKAI-UHFFFAOYSA-N
PubChem CID2793751
EC No.679-087-8
DTXSIDDTXSID10383154

Chemische & physikalische Eigenschaften

XLogP1,7
Polarare Oberfläche (TPSA)17,1
H-Brücken-Donoren0
H-Brücken-Akzeptoren1
Frei drehbare Bindungen1
Schwere Atome7
Formalladung0
Komplexität95
Siedepunkt71.5-72.5 °C(Press: 11 Torr)
Dichte1.2979 g/cm3
LöslichkeitMiscible with ethylene glycol and diethyl ether.

Sicherheit & Vorschriften

GHS-EinstufungDangerH314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]P260, P264, P280, P301+P330+P331, P302+P361+P354, P304+P340, P305+P354+P338, P316, P321, P363, P405, and P501 (click each P-code to see the statement)Aggregated GHS information provided per 4 reports by companies from 1 notifications to the ECHA C&L Inventory.Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
UN-TransportnummerUN3265
Gefahrenklasse8
VerpackungsgruppeII

Anwendungen & Verwendung

Verwenden

Isopropylphosphonic dichloride is used as a raw material for the preparation of bis(fluoroalkyl) alkylphosphonates by reacting with fluoroalcohols in the presence of triethylamine as catalyst.