Ethyl 2-(Diethoxyphosphoryl) acetate
diethyl (ethoxyacetyl)phosphonate
CAS: 30492-56-9
Molecular Formula: C8H17O5P
Ethyl 2-(Diethoxyphosphoryl) acetate - Names and Identifiers
| Name | diethyl (ethoxyacetyl)phosphonate |
| Synonyms | diethyl (ethoxyacetyl)phosphonate Diethyl (ethoxyacetyl)phosphonate Ethyl 2-(Diethoxyphosphoryl) acetate |
| CAS | 30492-56-9 |
| EINECS | 250-217-1 |
| InChI | InChI=1/C8H17O5P/c1-4-11-7-8(9)14(10,12-5-2)13-6-3/h4-7H2,1-3H3 |
Ethyl 2-(Diethoxyphosphoryl) acetate - Physico-chemical Properties
| Molecular Formula | C8H17O5P |
| Molar Mass | 224.19 |
| Density | 1.115g/cm3 |
| Melting Point | -24 °C |
| Boling Point | 262.3°C at 760 mmHg |
| Flash Point | 126.5°C |
| Vapor Presure | 0.011mmHg at 25°C |
| Storage Condition | Room Temprature |
| Refractive Index | 1.423 |
Ethyl 2-(Diethoxyphosphoryl) acetate - Introduction
diethyl (ethoxyacetyl) phosphate is an organophosphorus compound with the chemical formula C8H17O4P. It is a colorless liquid with a special smell.
diethyl (ethoxyacetyl)phosphonate is commonly used as a phosphating agent, buffer and catalyst. It can be used in the acyl transfer reactions of carboxylic esters in organic synthesis reactions and in the synthesis of other phosphates.
Preparation of diethyl (ethoxyacetyl) phosphate can be obtained by reacting ethyl bromoacetate with triethylphosphine under alkaline conditions. The reaction requires attention to safety, use appropriate personal protective equipment, and operate under well-ventilated conditions.
diethyl (ethoxyacetyl)phosphonate is less toxic, but care should be taken to avoid inhalation, skin contact and ingestion. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical assistance. During storage and handling, contact with strong oxidants, acids and bases should be avoided.
diethyl (ethoxyacetyl)phosphonate is commonly used as a phosphating agent, buffer and catalyst. It can be used in the acyl transfer reactions of carboxylic esters in organic synthesis reactions and in the synthesis of other phosphates.
Preparation of diethyl (ethoxyacetyl) phosphate can be obtained by reacting ethyl bromoacetate with triethylphosphine under alkaline conditions. The reaction requires attention to safety, use appropriate personal protective equipment, and operate under well-ventilated conditions.
diethyl (ethoxyacetyl)phosphonate is less toxic, but care should be taken to avoid inhalation, skin contact and ingestion. In case of contact with skin or eyes, rinse immediately with plenty of water and seek medical assistance. During storage and handling, contact with strong oxidants, acids and bases should be avoided.
Last Update：2024-04-10 22:29:15
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