1428677-26-2

Upstream product

• 1073-67-2 4-vinylbenzyl chloride 
• 7732-18-5 water 
• 1411983-70-4 bis[2-(4-chlorophenyl)ethyl]phosphine 

Downstream Products

• 1610599-61-5 2-butoxyethyl[bis(4-chlorophenethyl)]phosphine sulfide 
• 1610599-66-0 bis(4-chlorophenethyl)[2-(phenylsulfanyl)ethyl]phosphine sulfide 
• 1428677-27-3 C₃₂H₃₂Cl₄P₂S₂Se 
• 1428677-31-9 C₁₆H₁₇Cl₂PSSe 
• 1428677-31-9 C₁₆H₁₇Cl₂PSSe 
• 1443532-84-0 1-(2-furylmethoxy)ethyl bis(4-chlorophenethyl)phosphinothioselenoate 
• 1443532-85-1 1-(2-furylmethoxy)ethyl bis(4-chlorophenethyl)phosphinoselenothioate 
• 1443532-82-8 1-[(2,2,3,3-tetrafluoropropyl)oxy]ethyl bis(4-chlorophenethyl)phosphinothioselenoate 
• 1443532-83-9 1-[(2,2,3,3-tetrafluoropropyl)oxy]ethyl bis(4-chlorophenethyl)phosphinoselenothioate 

Relevant academic research and scientific papers

Atom-economic synthesis of highly branched functional tripod-like triphosphine sulfides

The tertiary polyfunctional triphosphine sulfides with amino and (or) ether groups have been synthesized in excellent yields by the exhaustive regioselective (in anti-Markovnikov manner) addition of secondary phosphines sulfides to trivinyl ethers of amin

Electrophilic addition of thioselenophosphinic acids to vinyl sulfides and selenides

The thioselenophosphinic acids, R2P(Se)SH (R = Ph, Cy, aralkyl), prepared by acidification of the sodium salts or generated in situ by reaction of secondary phosphine sulfides with elemental selenium, add easily to diverse vinyl sulfides and vi

Facile non-catalyzed synthesis of tertiary phosphine sulfides by regioselective addition of secondary phosphine sulfides to alkenes

An atom-economic green synthesis of tertiary phsophine sulfides has been developed based on catalyst- and solvent-free addition of secondary phosphine sulfides to diverse terminal and internal alkenes (hept-1-ene, cyclohexene, styrenes, allyl alcohol, vin