CAS 2524-64-3
:Diphenyl chlorophosphate
- 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
- See more synonyms
Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurity:>95.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight: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:C12H10ClO3PPurity:97%Color and Shape:Clear colorless, LiquidMolecular weight:268.63Diphenyl Chlorophosphate
CAS:Formula:C12H10ClO3PPurity:95%Color and Shape:LiquidMolecular weight:268.6328Diphenyl 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:C12H10ClO3PPurity:Min. 99.0 Area-%Color and Shape:Clear LiquidMolecular weight:268.63 g/molDiphenyl chlorophosphate
CAS:Formula:C12H10ClO3PPurity:95%Color and Shape:ClearMolecular weight:268.63Diphenyl Chlorophosphonate
CAS:Controlled ProductApplications 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:C12H10ClO3PColor and Shape:NeatMolecular weight:268.63Diphenyl Chlorophosphonate-d10
CAS:Controlled ProductFormula:C12D10ClO3PColor and Shape:NeatMolecular weight:278.694








