139-69-5

Upstream product

• 96-36-6 methyl phosphite 
• 108-93-0 cyclohexanol 
• 762-04-9 Diethyl phosphonate 
• 691-96-3 diisopropyl phosphite 
• 109-47-7 dibutyl hydrogen phosphite 

Downstream Products

• 95871-39-9 α-Anilino-benzyl-phosphonsaeure-O.O-dicyclohexylester 
• 23707-53-1 1.2-Bis--ethan 
• 92790-07-3 Propylphosphonsaeure-O_.O-dicyclohexylester-nitril 
• 97616-69-8 Propylphosphonsaeure-O_.O-dicyclohexylester-methylester 
• 98176-12-6 Isopropylphosphonsaeure-methylester-dicyclohexylester 
• 97117-73-2 α-(4-Nitro-anilino)-benzylphosphonsaeure-O.O-dicyclohexylester 
• 97357-27-2 α-(p-Toluidino-benzyl)-phosphonsaeure-O.O-dicyclohexylester 
• 1370555-10-4 O,O-dicyclohexyl S-methyl-d3 phosphorothioate 
• 1370554-99-6 O,O-dicyclohexyl S-methyl phosphorothioate 
• 1167445-05-7 dicyclohexyl [N,N-bis(2-ethylhexyl)aminomethyl]-phosphonate 
• 23489-39-6 1.2-Bis--ethan 
• 3011-80-1 methylenebis(dicyclohexyl phosphonate) 
• 100210-87-5 Isopropylphosphonsaeure-butylester-dicyclohexylester 

Relevant academic research and scientific papers

New synthesis of phosphorous and phosphoric acid esters

Reaction of alcohols with dialkyl phosphites in the presence of titanium tetraalkoxides results in a displacement of both or one ester function(s) by the RO groups of the alcohol used. The mixed phosphites, (R3O)(R1O)P(O)H, prepared by this method can be used as substrates for the mixed phosphates, (R4O)(R3O)(R1O)PO.