Ordering
Available Variants5 g
CHA.83109-5g
Price
€24.60
Available – Dispatch in 14 days
25 g
CHA.83109-25g
Price
€93.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.83109-5g | €24.60 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
25 g | CHA.83109-25g | €93.60 |
96%
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Linear Formula | CH3COCH2P(O)(OC2H5)2 |
|---|---|
| CAS Number | 1067-71-6 |
| Molecular Weight | 194.17 |
| NACRES | NA.22 |
| PubChem Substance ID | 24863071 |
| UNSPSC Code | 12352108 |
| MDL number | MFCD00044728 |
| Assay | 96% |
| Form | liquid |
Safety Information Handling visibility
| Storage Class | 10 - Combustible liquids |
|---|---|
| wgk | WGK 3 |
| flash_point_f | Not applicable |
| flash_point_c | Not applicable |
| ppe | Eyeshields, Gloves |
Technical Overview & Applications Use-case context
Diethyl (2-oxopropyl)phosphonate, with the CAS number 1067-71-6, is a chemical compound that has been utilized in various applications due to its unique properties. This phosphonate ester is known for its role as an intermediate in the synthesis of other compounds, particularly in the production of pharmaceuticals and agrochemicals. Its chemical structure, consisting of a phosphonate group attached to a 2-oxopropyl moiety, allows it to participate in a range of reactions, including nucleophilic substitutions and additions. As a result, diethyl (2-oxopropyl)phosphonate has become a valuable reagent in organic synthesis, enabling the creation of complex molecules with specific functional groups. Its reactivity and versatility make it a useful tool for chemists and researchers in various fields, contributing to advancements in fields such as medicine and agriculture.
