79296-58-5

Basic information

• Product Name: [hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid dimethyl ester
• CAS NO: 79296-58-5
• Molecular Weight: 246.2
• Mol File: 79296-58-5.mol
• Article Data: 25

Chemical Properties

• CAS DataBase Reference: [hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid dimethyl ester(79296-58-5)
• EPA Substance Registry System: [hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid dimethyl ester(79296-58-5)

Safety Data

• Hazardous Substances Data: 79296-58-5(Hazardous Substances Data)

Upstream product

• 10570-48-6 dimethyl 4-methoxybenzoylphosphonate 
• 2033-24-1 cycl-isopropylidene malonate 
• 123-11-5 4-methoxy-benzaldehyde 
• 121-45-9 phosphorous acid trimethyl ester 
• 96-36-6 methyl phosphite 
• 36198-87-5 dimethyl trimethylsilyl phosphite 
• 100-07-2 4-methoxy-benzoyl chloride 
• 868-85-9 Dimethyl phosphite 

Downstream Products

• 1000281-15-1 chloro-acetic acid (dimethoxy-phosphoryl)-(4-methoxy-phenyl)-methyl ester 
• 1332458-73-7 (dimethoxyphosphoryl)(4-methoxyphenyl)methyl 2-(4,6-dimethoxypyrimidin-2-yloxy)benzoate 
• 63694-17-7 (4-methoxyphenyl)(hydroxy)methylphosphonic acid 
• 1207757-83-2 O,O-dimethyl-2,6-pyridinyldi(formyloxy-4-methoxybenzylphosphonate) 
• 1208065-70-6 dimethyl [(2-methoxyphenyl)(6-oxo-6λ5-dibenzo[d,f][1,3,2]dioxaphosphepin-6-yl)ethyl]phosphonate 
• 79296-53-0 [Hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid monomethyl ester 
• 694489-32-2 (2,4-dichloro-phenoxy)-acetic acid (dimethoxy-phosphoryl)-(4-methoxy-phenyl)-methyl ester 
• 79296-53-0 [Hydroxy-(4-methoxy-phenyl)-methyl]-phosphonic acid monomethyl ester 
• 125172-85-2 P-[2-(4-methylphenyl)ethynyl] dimethyl phosphonate 
• 1352612-27-1 (dimethoxyphosphoryl)(4-methoxyphenyl)methyl cinnamate 

Relevant articles and documents

Biocatalytic Promiscuity of Lipases in Carbon-Phosphorus Bond Formation

A promiscuous lipase-catalyzed carbon-phosphorus bond formation is presented. The developed enzymatic Pudovik-Abramov reaction of various aromatic and aliphatic aldehydes with dialkyl phosphonates provides biologically and pharmacologically relevant α-hyd

Ultrasound assisted green synthesis of α-hydroxyphosphonates under solvent-free conditions

Abstract: A simple, efficient and environmentally benign method for the synthesis of α-hydroxyphosphonates by reaction of an aldehyde or a ketone, and trialkylphosphite is effectively accomplished under ultrasound irradiation and solvent-free and catalyst

Phospha-Michael Addition to in Situ Prepared 5-Arylmethylidene Meldrum's Acids

Knoevenagel condensation reaction of an aldehyde and Meldrum's acid produces a 5-arylmethylidene Meldrum's acid, which undergoes Michael addition of a trialkyl phosphite under solvent-free conditions to afford the title compounds in good yields.