CAS 1067-74-9
:Acetato de metilo (dietilfosfono)
Descripción:
Acetato de metilo (dietilfosfono), con el número CAS 1067-74-9, es un compuesto organofosforado caracterizado por sus grupos funcionales de éster y su estructura de fosfonato. Típicamente aparece como un líquido incoloro a amarillo pálido con un olor distintivo. Este compuesto es conocido por sus aplicaciones en la síntesis orgánica, particularmente como un intermedio en la producción de varios productos farmacéuticos y agroquímicos. Acetato de metilo (dietilfosfono) exhibe una solubilidad moderada en disolventes orgánicos, mientras que su solubilidad en agua es limitada. Es relativamente estable en condiciones normales, pero puede sufrir hidrólisis en presencia de ácidos o bases fuertes. El compuesto también es reconocido por su potencial toxicidad, lo que requiere un manejo cuidadoso y medidas de seguridad adecuadas durante su uso. Su reactividad está influenciada por la presencia del grupo fosfonato, que puede participar en reacciones de sustitución nucleofílica. En general, Acetato de metilo (dietilfosfono) es un químico versátil con una relevancia significativa en la química sintética y aplicaciones industriales.
Fórmula:C7H15O5P
InChI:InChI=1S/C7H15O5P/c1-4-11-13(9,12-5-2)6-7(8)10-3/h4-6H2,1-3H3
Clave InChI:InChIKey=CTSAXXHOGZNKJR-UHFFFAOYSA-N
SMILES:P(CC(OC)=O)(OCC)(OCC)=O
Sinónimos:- (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
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Encontrado 8 productos.
Methyl Diethylphosphonoacetate
CAS:Fórmula:C7H15O5PPureza:>96.0%(GC)Forma y color:Colorless to Almost colorless clear liquidPeso molecular: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>Fórmula:C7H15O5PPureza:97%Forma y color:Clear colorless, LiquidPeso molecular:210.17Methyl diethylphosphonoacetate
CAS:Fórmula:C7H15O5PPureza:97%Forma y color:LiquidPeso molecular:210.1648Diethyl (methoxycarbonylmethyl)phosphonate
CAS:<p>Diethyl (methoxycarbonylmethyl)phosphonate</p>Fórmula:C7H15O5PPureza:98%Forma y color: colourless liquidPeso molecular:210.16g/molMethyl 2-(diethoxyphosphoryl)acetate
CAS:Fórmula:C7H15O5PPureza:95%Forma y color:Liquid, ClearPeso molecular:210.166Methyl Diethylphosphonoacetate-D2
CAS:Producto controladoFórmula:C7D2H13O5PForma y color:NeatPeso molecular:212.177Methyl Diethylphosphonoacetate
CAS:Producto controlado<p>Applications Methyl Diethylphosphonoacetate (cas# 1067-74-9) is a useful research chemical.<br></p>Fórmula:C7H15O5PForma y color:NeatPeso molecular: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>Fórmula:C7H15O5PPureza:Min. 95%Peso molecular:210.16 g/mol







