CAS 1067-74-9
:Acetato de metila (dietilfosfono)
Descrição:
Acetato de metila (dietilfosfono), com o número CAS 1067-74-9, é um composto organofosforado caracterizado por seus grupos funcionais de éster e estrutura de fosfonato. Normalmente aparece como um líquido incolor a amarelo pálido com um odor distinto. Este composto é conhecido por suas aplicações na síntese orgânica, particularmente como um intermediário na produção de vários produtos farmacêuticos e agroquímicos. Acetato de metila (dietilfosfono) exibe solubilidade moderada em solventes orgânicos, enquanto sua solubilidade em água é limitada. É relativamente estável em condições normais, mas pode sofrer hidrólise na presença de ácidos ou bases fortes. O composto também é reconhecido por sua potencial toxicidade, exigindo manuseio cuidadoso e medidas de segurança adequadas durante o uso. Sua reatividade é influenciada pela presença do grupo fosfonato, que pode participar de reações de substituição nucleofílica. No geral, Acetato de metila (dietilfosfono) é um químico versátil com relevância significativa na química sintética e aplicações industriais.
Fórmula:C7H15O5P
InChI:InChI=1S/C7H15O5P/c1-4-11-13(9,12-5-2)6-7(8)10-3/h4-6H2,1-3H3
Chave 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
- Ver mais sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
8 produtos.
Methyl Diethylphosphonoacetate
CAS:Fórmula:C7H15O5PPureza:>96.0%(GC)Cor e Forma: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%Cor e Forma:Clear colorless, LiquidPeso molecular:210.17Methyl diethylphosphonoacetate
CAS:Fórmula:C7H15O5PPureza:97%Cor e Forma:LiquidPeso molecular:210.1648Diethyl (methoxycarbonylmethyl)phosphonate
CAS:Diethyl (methoxycarbonylmethyl)phosphonateFórmula:C7H15O5PPureza:98%Cor e Forma: colourless liquidPeso molecular:210.16g/molMethyl 2-(diethoxyphosphoryl)acetate
CAS:Fórmula:C7H15O5PPureza:95%Cor e Forma:Liquid, ClearPeso molecular:210.166Methyl Diethylphosphonoacetate-D2
CAS:Produto ControladoFórmula:C7D2H13O5PCor e Forma:NeatPeso molecular:212.177Methyl Diethylphosphonoacetate
CAS:Produto Controlado<p>Applications Methyl Diethylphosphonoacetate (cas# 1067-74-9) is a useful research chemical.<br></p>Fórmula:C7H15O5PCor e Forma:NeatPeso molecular:210.16Methyl diethylphosphonoacetate
CAS: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.Fórmula:C7H15O5PPureza:Min. 95%Peso molecular:210.16 g/mol







