Diphenyl chlorophosphate

CAS: 2524-64-3

Ref. 3D-FD32930

Información del producto

• Nombre: Diphenyl chlorophosphate
• Sinónimos: Chlorodiphenoxyphosphine oxide, Chlorophosphonic acid diphenyl ester, Chlorophosphoric Acid Diphenyl Ester, DCP, DPC, DPC (flame retardant), Diphenoxychlorophosphine oxide, Diphenyl Ester, Diphenyl Phosphorochloridoite, Diphenyl Phosphoryl Chloride, Diphenyl chloridophosphate, Diphenyl chlorophosphonate, Diphenyl phosphate chloride, Diphenyl phosphochloridate, Diphenyl phosphorochlorate, Diphenyl phosphorochloridate, Diphenyl phosphorochoridate, Diphenylchlorophosphonate, Diphenylchlorphosphat, Diphenylphosphoric acid monochloride, Diphenylphosphorus oxychloride, Diphenylphosphoryl Chloride, Diphenylphosphoryl monochloride, Dpcp, Dppc, Fosforocloridato De Difenilo, Nsc 43771, O,O-Diphenyl chlorophosphate, Phenyl phosphorochloridate ((PhO)2ClPO), Phenyl phosphorochloridate ((PhO)₂ClPO), Phenyl phosphorochloridite, Phosphoric Acid Diphenyl Ester Chloride, Phosphoric acid chloride diphenyl ester, Phosphorochloridate de diphenyle, Phosphorochloridic acid diphenyl ester, [Chloro(phenoxy)phosphoryl]oxybenzene

Descripción

Diphenyl chlorophosphate is a reactive molecule that is classified as an organic compound. It has been synthesized in vitro by reacting sodium carbonate with p-hydroxybenzoic acid and trifluoroacetic acid. The synthesis of this compound was successful because the hydroxyl group on p-hydroxybenzoic acid reacted with the amide group on sodium carbonate to form an amide linkage. This reaction also created an alkanoic acid, which was hydrolyzed to form an ester linkage between the two molecules. Diphenyl chlorophosphate has been shown to bind to receptor molecules and inhibit their activity, which may be due to its ability to react with other molecules in order to produce a new product.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 268.63 g/mol
• Fórmula: C₁₂H₁₀ClO₃P
• Pureza: Min. 99.0 Area-%
• Color/Forma: Clear Liquid