CAS 2524-64-3
:Clorofosfato di difenile
- 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)<sub>2</sub>ClPO)
- Phenyl phosphorochloridite
- Phosphoric Acid Diphenyl Ester Chloride
- Phosphoric acid chloride diphenyl ester
- Phosphorochloridate de diphenyle
- Phosphorochloridic acid diphenyl ester
- Vedi altri sinonimi
Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurezza:>95.0%(GC)Colore e forma:Colorless to Light yellow clear liquidPeso molecolare:268.63Diphenyl phosphorochloridate, 97%
CAS:Diphenyl phosphorochloridate is used to prepare cyclohexyl-amidophosphoric acid diphenyl ester by reacting with cyclohexylamine. It is also used in the synthesis of alfa-substituted beta-lactams, anhydrides, esters and thioesters. It is also employed in the conversion of aldoximes to nitriles. Furth
Formula:C12H10ClO3PPurezza:97%Colore e forma:Clear colorless, LiquidPeso molecolare:268.63Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurezza:95%Colore e forma:LiquidPeso molecolare:268.6328Ref: 4Z-R-3913
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaDiphenyl chlorophosphate
CAS: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.
Formula:C12H10ClO3PPurezza:Min. 99.0 Area-%Colore e forma:Clear LiquidPeso molecolare:268.63 g/molDiphenyl chlorophosphate
CAS:Formula:C12H10ClO3PPurezza:95%Colore e forma:ClearPeso molecolare:268.63Diphenyl Chlorophosphonate
CAS:Prodotto controllatoApplications Diphenyl Chlorophosphonate, is a building block used for the synthesis of various chemical compounds. It can be used for the synthesis of phosphate esters of polyhedral hydroxyboranes, showing enhanced tumor uptake.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Bechtold, R., et al.: J. Med. Chem., 18, 371 (1975);Formula:C12H10ClO3PColore e forma:NeatPeso molecolare:268.63Diphenyl Chlorophosphonate-d10
CAS:Prodotto controllatoFormula:C12D10ClO3PColore e forma:NeatPeso molecolare:278.694Ref: ST-EA-CP-R31014
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