≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
application：
Reactant for synthesis of:
Sulfonyl hydroxamate derivatives for use as inhibitors of class ii fructosediphosphate aldolase
Imidazole glycerol phosphate dehydratase inhibitors
Competitive N-methyl-D-aspartate antagonists with analgesic activity
Farnesyl phosphonate derivatives of phenylalanine for inhibition of farnesyl protein transferase
Reactant for condensation reactions with isobutyraldehyde。
| Pubchem Sid | 488189238 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488189238 |
| Sonrisas canónicas | CCOC(=O)CCP(=O)(OCC)OCC |
| IUPAC Name | ethyl 3-diethoxyphosphorylpropanoate |
| InChIKey | JMJWCUOIOKBVNQ-UHFFFAOYSA-N |
| INCHI | 1S/C9H19O5P/c1-4-12-9(10)7-8-15(11,13-5-2)14-6-3/h4-8H2,1-3H3 |
| Isómeros SMILES | CCOC(=O)CCP(=O)(OCC)OCC |
| WGK Alemania | 3 |
| PubChem CID | 281204 |
| Peso molecular | 238.22 |
| Reaxy-Rn | 1790966 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Clase | Organic phosphonic acids and derivatives |
| Subclass | Phosphonic acid diesters |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Dialkyl alkylphosphonates |
| Alternative Parents | Phosphonic acid esters Carboxylic acid esters Monocarboxylic acids and derivatives Organopnictogen compounds Organophosphorus compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Dialkyl alkylphosphonate - Phosphonic acid ester - Carboxylic acid ester - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as dialkyl alkylphosphonates. These are compounds containing a phosphonic acid that is diesterified with alkyl groups, and the phosphorus atom is also directly attached to an alkyl group. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 K2109511 | Certificate of Analysis | Aug 20, 2025 | T161842 |
| K2109512 | Certificate of Analysis | Aug 20, 2025 | T161842 |
| K2109513 | Certificate of Analysis | Aug 20, 2025 | T161842 |
| K2109515 | Certificate of Analysis | Aug 20, 2025 | T161842 |
| Índice de refracción | 1.43 |
|---|---|
| Punto de inflamación (°F) | >235.4 °F |
| Punto de inflamación (°C) | >113 °C |
| Punto de ebullición (°C) | 95°C/1mmHg(lit.) |
| Peso molecular | 238.220 g/mol |
| XLogP3 | 0.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 9 |
| Exact Mass | 238.097 Da |
| Monoisotopic Mass | 238.097 Da |
| Topological Polar Surface Area | 61.800 Ų |
| Heavy Atom Count | 15 |
| Formal Charge | 0 |
| Complexity | 219.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
