17105-65-6

Basic information

• Product Name: DIMETHYL(4-METHOXYBENZYL)PHOSPHONATE
• Synonyms: DIMETHYL(4-METHOXYBENZYL)PHOSPHONATE
• CAS NO: 17105-65-6
• Molecular Formula: C₁₀H₁₅O₄P
• Molecular Weight: 230.2
• Mol File: 17105-65-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DIMETHYL(4-METHOXYBENZYL)PHOSPHONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL(4-METHOXYBENZYL)PHOSPHONATE(17105-65-6)
• EPA Substance Registry System: DIMETHYL(4-METHOXYBENZYL)PHOSPHONATE(17105-65-6)

Safety Data

• Hazardous Substances Data: 17105-65-6(Hazardous Substances Data)

Upstream product

• 868-85-9 Dimethyl phosphite 
• 270921-39-6 (4-methoxyphenyl)methyl methyl carbonate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 123-11-5 4-methoxy-benzaldehyde 
• 2746-25-0 p-Methoxybenzyl bromide 
• 121-45-9 phosphorous acid trimethyl ester 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 158751-23-6 2-Benzyloxy-1-methoxy-3-[(E)-2-(4-methoxy-phenyl)-vinyl]-benzene 
• 86457-76-3 Dimethyl 1-chloro-1-(4-methoxyphenyl)methanephosphonate 
• 1694-19-5 E-1-(phenyl)-2-(4'-methoxyphenyl)ethene 
• 79958-53-5 (E)-1-(3,3-dimethylbut-1-en-1-yl)-4-methoxybenzene 
• 72078-54-7 4-methoxy-4'-methylstilbene 
• 2746-25-0 p-Methoxybenzyl bromide 
• 22145-08-0 1-(4-methoxyphenyl)-4-phenyl-1,3-butadiene 
• 43212-67-5 1-(4-methoxyphenyl)-4-(4-methoxyphenyl)-1,3-butadiene 
• 569-57-3 chlorotrianisene 
• 158751-26-9 [3-(2-(Tetrahydro-pyran-2-yloxy)-6-{2-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-ethyl}-phenoxy)-benzyl]-phosphonic acid dimethyl ester 
• 246257-37-4 C₃₁H₃₅BrO₅ 
• 158751-24-7 3-{2-Methoxy-6-[2-(4-methoxy-phenyl)-ethyl]-phenoxy}-benzaldehyde 
• 158751-25-8 2-(3-Bromomethyl-phenoxy)-3-[2-(4-hydroxy-phenyl)-ethyl]-phenol 
• 246257-34-1 2-[3-(hydroxymethyl)phenoxy]-3-[2-(4-hydroxyphenyl)ethyl]phenol 

Relevant articles and documents

Synthesis of α-Aryldiazophosphonates via a Diazo Transfer Reaction

The simple synthetic procedure for preparation of α-aryl-α-diazophosphonates via a diazo transfer reaction is proposed. Benzylphosphonates reacted with tosyl azide (TsN3) in the presence of potassium tert-butoxide (KOtBu) to afford diazophosphonates in a yield up to 79%. The proposed method is general. The reaction uses easily available starting materials, tolerates various functional groups, and may be applied for multi-gram scale synthesis.

Synthesis of Trisubstituted Vinyl Chlorides

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