52925-84-5

Basic information

• Product Name: diethyl 1,1,3,3,3-pentachloroprop-1-en-2-yl phosphate
• Synonyms: Diethyl 1,1,3,3,3-pentachloroprop-1-en-2-yl phosphate; phosphoric acid, 2,2-dichloro-1-(trichloromethyl)ethenyl diethyl ester
• CAS NO: 52925-84-5
• Molecular Formula: C₇H₁₀Cl₅O₄P
• Molecular Weight: 366.3907
• Mol File: 52925-84-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 298.2°C at 760 mmHg
• Flash Point: 171.8°C
• Density: 1.542g/cm³
• Vapor Pressure: 0.00228mmHg at 25°C
• Refractive Index: 1.505
• CAS DataBase Reference: diethyl 1,1,3,3,3-pentachloroprop-1-en-2-yl phosphate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl 1,1,3,3,3-pentachloroprop-1-en-2-yl phosphate(52925-84-5)
• EPA Substance Registry System: diethyl 1,1,3,3,3-pentachloroprop-1-en-2-yl phosphate(52925-84-5)

Safety Data

• Hazardous Substances Data: 52925-84-5(Hazardous Substances Data)

Upstream product

• 762-04-9 phosphonic acid diethyl ester 
• 116-16-5 1,1,1,3,3,3-hexachloro-propan-2-one 

Relevant articles and documents

Nucleoside Phosphonates: Part 7. Studies on the Oxidation of Nucleoside Phosphonate Esters

Oxidation of phosphonate mono- and di-esters with various oxidizing agents including diaryl disulphides, hexacloroacetone, and iodine, has been investigated under various reaction conditions.The most efficient oxidation procedure consists of treatment of phosphonate esters with iodine in pyridine-water.When the phosphonate esters were presilylated by treatment with trimethylsilyl chloride, the subsequent oxidation with aqueous iodine was faster. (31)P N.m.r. spectroscopic studies have enabled us to propose the most likely pathway for the majority of the oxidations.