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HCID 69629Erstellt: 25. Oktober 2026

Diethylvinylphosphonat

2-ethylbut-1-enyl-dioxido-oxophosphorane · AURORA KA-1438 · diethylvinylphosphate · Diethyl vinylphosphate · Diethylevinylphosphonate · DIETHYL VINYLPHOSPHONATE · Diethoxyphosphinylethene · 1-diethoxyphosphorylethene

https://huagongshe.com/de/chemical/69629

Molekülstruktur von Diethylvinylphosphonat

Identifikatoren & physikalische Daten

CAS No.682-30-4
SummenformelC6H13O3P
Durchschnittliche Molmasse164,14 g/mol
Monoisotopische Masse164,06023091 g/mol
SMILESC=CP(=O)(OCC)OCC
InChIKeyDREPONDJUKIQLX-UHFFFAOYSA-N
PubChem CID69629
EC No.211-663-2
DTXSIDDTXSID70218372
Lokaler NameDiethylvinylphosphonat

Chemische & physikalische Eigenschaften

XLogP0,7
Polarare Oberfläche (TPSA)35,5
H-Brücken-Donoren0
H-Brücken-Akzeptoren3
Frei drehbare Bindungen5
Schwere Atome10
Formalladung0
Komplexität134
SpringerMaterials Properties31P nuclear magnetic resonance spectrum
Siedepunkt202 °C(lit.)
Dichte1.068 g/mL at 25 °C(lit.)
Brechungsindexn20/D 1.429(lit.)
Flammpunkt>230 °F
Lagerbedingungen2-8°C
AggregatzustandLiquid
FarbeClear colorless to light yellow
Wichte1.068
BRN507596
InChIInChI=1S/C6H13O3P/c1-4-8-10(7,6-3)9-5-2/h6H,3-5H2,1-2H3
InChIKeyDREPONDJUKIQLX-UHFFFAOYSA-N
SMILESP(C=C)(=O)(OCC)OCC
CAS Datenbank682-30-4

Sicherheit & Vorschriften

GHS-EinstufungDangerH301 (100%): Toxic if swallowed [Danger Acute toxicity, oral]P264, P270, P301+P316, P321, P330, 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.
F10
Wassergefährdungsklasse (WGK)3
UN-TransportnummerUN3278
Zollcode29319090
RTECS-Nr.TA1150000
GefahrensymboleT
hazard_noteToxic
Sicherheitshinweise (S)23-24/25
Gefahrenklasse6.1
VerpackungsgruppeIII
Lagerklasse10 - Combustible liquids

Anwendungen & Verwendung

Verwenden

Diethyl vinylphosphonate (DEVP) can be used as a precursor for the synthesis of: α, β-unsaturated phosphonates by reacting with arylboronic acids via Pd-catalyzed MizorokiHeck reaction.2-(arylamino)ethyl phosphonates by condensing with primary and secondary amines via the aza-Michael addition reaction.It can be also employed as a monomer unit for the preparation of high-molecular-weight polymer, poly(diethyl vinylphosphonate)using lanthanide complexes.{18)

Diethyl vinylphosphonate|Huagongshe