67502-51-6

Basic information

• Product Name: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester
• CAS NO: 67502-51-6
• Molecular Formula: C11H17O3PSe
• Molecular Weight: 307.188
• Mol File: 67502-51-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(67502-51-6)
• EPA Substance Registry System: Phosphonic acid, [(phenylseleno)methyl]-, diethyl ester(67502-51-6)

Safety Data

• Hazardous Substances Data: 67502-51-6(Hazardous Substances Data)

Upstream product

• 20343-90-2 bis(phenylseleno)methane 
• 814-49-3 diethyl chlorophosphate 
• 10419-77-9 diethyl iodomethanephosphonate 
• 34837-55-3 Phenylselenyl bromide 
• 110625-05-3 diethyl-1-magnesium chloride methanephosphonate 
• 23974-72-3 sodium phenylselenide 
• 5707-04-0 Phenylselenyl chloride 
• 645-96-5 Benzeneselenol 
• 1666-13-3 diphenyl diselenide 

Downstream Products

• 60466-41-3 (E)-1-(phenylselenenyl)-2-(4-methylphenyl)ethene 
• 110339-19-0 1-Chloro-4-((Z)-2-chloro-2-phenylselanyl-vinyl)-benzene 
• 134891-99-9 diethyl <(3-oxo-1-cyclohexen-1-yl)methyl>phosphonate 
• 108365-51-1 (2,2-diphenylvinyl)(phenyl)selane 
• 60466-46-8 1-Methyl-4-((E)-2-phenylselanyl-propenyl)-benzene 
• 67502-58-3 C₁₆H₁₆Se 
• 130646-84-3 C₁₈H₂₀Se 
• 67502-69-6 (1-Cyclohexylidene-ethylselanyl)-benzene 
• 60466-35-5 phenyl 1-phenyl-2-propenyl selenide 
• 110339-17-8 5-((Z)-2-Chloro-2-phenylselanyl-vinyl)-benzo[1,3]dioxole 
• 110339-16-7 phenyl <1-chloro-2-(p-methoxyphenyl)ethenyl>-1-yl selenide 
• 110339-18-9 1-Chloro-3-((Z)-2-chloro-2-phenylselanyl-vinyl)-benzene 
• 110339-24-7 (Chloro-cyclohexylidene-methylselanyl)-benzene 
• 67502-52-7 diethyl 1-phenylselenenylethylphosphonate 

Relevant articles and documents

Direct and straightforward transfer of C1 functionalized synthons to phosphorous electrophiles for accessinggem-P-containing methanes

The direct transfer of different α-substituted methyllithium reagents to chlorinated phosphorous electrophiles of diverse oxidation state (phosphates, phosphine oxides and phosphines) is proposed as an effective strategy to synthesize geminal P-containing

ULTRASONIC FORMATION AND REACTIONS OF SODIUM PHENYLSELENIDE

Treatment of diphenyldiselenide with sodium metal in tetrahydrofuran under ultrasonic conditions conveniently gave a suspension of sodium phenylselenide which could be transferred by syringe or cannula and reacted with sulphonates, halides and epoxides.