Diethyl (cyanomethyl)phosphonate
Nome do item: Diethyl (cyanomethyl)phosphonate
Grupo: Other Specialties
Número CAS: 2537-48-6
Número EC: 219-806-0
Sinônimos:

ethyl dichlorophosphate, Cyanomethylphosphonic Acid Diethyl Ester, Diethyl cyanomethyl phosphonate, O,O-diethyl cyanomethylphosphonate, diethyl cyanomethanephosphonate, Diethyl CyanoMethylphosphonate, Diethyl (cyanomethyl)phosphonate, Diethylphosphonoacetonitrile, Cyanomethanephosphonic acid,diethyl ester, Diethyl cyanomethylphosphonate

Nome IUPAC: 2-diethoxyphosphorylacetonitrile
Fórmula molecular: C6H12NO3P
Peso molecular: 177.138 g/mol
Ponto de ebulição: 101-102ºC (0.4 mmHg)
Ponto de inflamação: 117.3ºC
Densidade: 1.095
Classe de perigo: 6.1
Código HS: 29310095
RID/ADR: UN 1760
Declarações de risco: R20/21/22; R36/37/38
Sinais: Warning

Fornecedor(es): 23

Diethyl (cyanomethyl)phosphonate
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Diethyl cyanomethylphosphonate
Product Name: Diethyl cyanomethylphosphonate Synonyms: (Cyanomethyl)diethoxyphosphine oxide;2-(Diethylphosphonyl)acetonitrile;Diethyl cyanomethanephosphonate;Phosphonic acid, (cyanomethyl)-, diethyl ester;Cyanomethylphosphonic acid diethyl ester~Diethyl phosphonoacetonitrile;Diethylcyanomethylphosphonate,98+%;Diethyl (cyanomethyl)phosphonate 98%;LABOTEST-BB LT00233137 CAS: 2537-48-6 MF: C6H12NO3P MW: 177.14 EINECS: 219-806-0 Product Categories: Pyridines;Wittig Reagents;Phosphorus compounds;Horner-Emmons Reaction;Synthetic Organic Chemistry;Wittig & Horner-Emmons Reaction Mol File: 2537-48-6.mol
Pharmaceutics
99%
TT Advance
CIF
SUZHOU, CHINA
Aplicação:
Diethyl cyanomethyl phosphonate is used as an intermediate in Horner-Emmons reaction for the synthesis of substituted nitriles and their amide and heterocyclic derivatives. It is known as a modified Wittig reagent used in the preparation of alpha, beta-unsaturated nitriles from ketones or aldehydes like 3-hydroxy-3-methylbutanal. It reacts with epoxides and nitrones to prepare cyano-substituted cyclopropanes and aziridines respectively. It is actively involved in the synthesis of alpha-arylated alkanenitriles via reaction with aryl iodides in presence of CuI.
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