CAS 1067-74-9
:Methyl (diethylphosphono)acetate
Description:
Methyl (diethylphosphono)acetate, with the CAS number 1067-74-9, is an organophosphorus compound characterized by its ester functional groups and phosphonate structure. It typically appears as a colorless to pale yellow liquid with a distinctive odor. This compound is known for its applications in organic synthesis, particularly as an intermediate in the production of various pharmaceuticals and agrochemicals. Methyl (diethylphosphono)acetate exhibits moderate solubility in organic solvents, while its solubility in water is limited. It is relatively stable under normal conditions but may undergo hydrolysis in the presence of strong acids or bases. The compound is also recognized for its potential toxicity, necessitating careful handling and appropriate safety measures during use. Its reactivity is influenced by the presence of the phosphonate group, which can participate in nucleophilic substitution reactions. Overall, Methyl (diethylphosphono)acetate is a versatile chemical with significant relevance in synthetic chemistry and industrial applications.
Formula:C7H15O5P
InChI:InChI=1S/C7H15O5P/c1-4-11-13(9,12-5-2)6-7(8)10-3/h4-6H2,1-3H3
InChI key:InChIKey=CTSAXXHOGZNKJR-UHFFFAOYSA-N
SMILES:P(CC(OC)=O)(OCC)(OCC)=O
Synonyms:- (Diethoxyphosphinyl)acetic acid methyl ester
- (Methoxycarbonylmethyl) diethoxyphosphine oxide
- Acetic acid, (diethoxyphosphinyl)-, methyl ester
- Acetic acid, 2-(diethoxyphosphinyl)-, methyl ester
- Acetic acid, phosphono-, P,P-diethyl methyl ester
- Acetic acid, phosphono-, diethyl 1-methyl ester
- Diethyl (methoxycarbonylmethyl)phosphonate
- Diethyl carbomethoxymethylphosphonate
- Diethyl methoxycarbonylmethanephosphonate
- Diethyl methoxycarbonylmethyl phosphonate~Phosphonoacetic acid diethyl methyl ester
- Diethyl phosphonate, methoxycarbonylmethyl-
- Diethylphosphonoacetic acid methyl ester
- Methoxycarbonylmethanephosphonic acid diethyl ester
- Methyl (Diethoxyphosphoryl)Acetate
- Methyl (diethoxyphosphinyl)acetate
- Methyl (diethylphosphono)acetate
- Methyl 2-(diethoxyphosphinyl)acetate
- Methyl 2-(diethoxyphosphono)acetate
- Methyl 2-(diethoxyphosphoryl)acetate
- Methyl 2-(diethylphosphonato)acetate
- Methyl 2-(diethylphosphono)acetate
- Methyl di-O-ethylphosphonoacetate
- Methyl diethoxyphosphonoacetate
- NSC 147757
- O,O-Diethyl phosphonoacetic acid methyl ester
- Pome
- [(Methoxycarbonyl)-methyl]-phosphonic acid diethyl ester
- See more synonyms
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Found 8 products.
Methyl Diethylphosphonoacetate
CAS:Formula:C7H15O5PPurity:>96.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:210.17Methyl diethylphosphonoacetate, 97%
CAS:<p>Methyl diethylphosphonoacetate is used as a reagent in the preparation of allylic fluorides compounds and in regioselective Diels-Alder reactions. It also serves as a reactant in the preparation of substituted thiophenes and furans, which finds application in type 2 diabetes treatment. Further, it a</p>Formula:C7H15O5PPurity:97%Color and Shape:Clear colorless, LiquidMolecular weight:210.17Methyl diethylphosphonoacetate
CAS:Formula:C7H15O5PPurity:97%Color and Shape:LiquidMolecular weight:210.1648Diethyl (methoxycarbonylmethyl)phosphonate
CAS:<p>Diethyl (methoxycarbonylmethyl)phosphonate</p>Formula:C7H15O5PPurity:98%Color and Shape: colourless liquidMolecular weight:210.16g/molMethyl 2-(diethoxyphosphoryl)acetate
CAS:Formula:C7H15O5PPurity:95%Color and Shape:Liquid, ClearMolecular weight:210.166Methyl Diethylphosphonoacetate-D2
CAS:Controlled ProductFormula:C7D2H13O5PColor and Shape:NeatMolecular weight:212.177Methyl Diethylphosphonoacetate
CAS:Controlled Product<p>Applications Methyl Diethylphosphonoacetate (cas# 1067-74-9) is a useful research chemical.<br></p>Formula:C7H15O5PColor and Shape:NeatMolecular weight:210.16Methyl diethylphosphonoacetate
CAS:<p>Methyl diethylphosphonoacetate is a chemical compound that contains a hydroxy group, an alkynyl group and a disulfide bond. It is used as a control agent in the production of polyurethane foams, and has also been shown to inhibit the growth of bladder cancer cells. The UV absorption peak at 220 nm can be used to identify this chemical compound. Methyl diethylphosphonoacetate reacts with proton to form diethylphosphonoacetate, which then undergoes an elimination reaction with fatty acids to form aliphatic hydrocarbons. This reaction mechanism was first proposed by Stork and co-workers in 1960. Methyl diethylphosphonoacetate also binds to thrombin receptor, which may lead to anti-inflammatory effects.</p>Formula:C7H15O5PPurity:Min. 95%Molecular weight:210.16 g/mol







