79158-40-0

Basic information

• Product Name: Phosphonic acid, [hydroxy(4-methylphenyl)methyl]-, diethyl ester
• CAS NO: 79158-40-0
• Molecular Formula: C12H19O4P
• Molecular Weight: 258.254
• Mol File: 79158-40-0.mol
• Article Data: 50

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [hydroxy(4-methylphenyl)methyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [hydroxy(4-methylphenyl)methyl]-, diethyl ester(79158-40-0)
• EPA Substance Registry System: Phosphonic acid, [hydroxy(4-methylphenyl)methyl]-, diethyl ester(79158-40-0)

Safety Data

• Hazardous Substances Data: 79158-40-0(Hazardous Substances Data)

Upstream product

• 2942-54-3 diethyl (4-methylbenzoyl)phosphonate 
• 104-87-0 4-methyl-benzaldehyde 
• 122-52-1 triethyl phosphite 
• 762-04-9 Diethyl phosphonate 
• 2033-24-1 cycl-isopropylidene malonate 
• 762-04-9 phosphonic acid diethyl ester 
• 96258-65-0 diethyl α-trimethylsilyloxy-4-methylbenzylphosphonate 

Downstream Products

• 96258-65-0 diethyl α-trimethylsilyloxy-4-methylbenzylphosphonate 
• 26321-53-9 diethyl (phenylamino)(p-tolyl)methylphosphonate 
• 1181811-95-9 diethyl α,α-chlorofluoro-4-methylbenzylphosphonate 
• 104561-47-9 diethyl α-chloro-4-methylbenzylphosphonate 
• 1322881-47-9 diethyl [(anilinocarbonyl)oxy](p-methylphenyl)methyl phosphonate 
• 185965-95-1 (difluoro-p-tolylmethyl)phosphonic acid diethyl ester 
• 1408232-38-1 C₂₀H₁₆F₂N₃O₃P 
• 1408232-39-2 C₂₄H₂₄F₂N₃O₃P 
• 1408232-42-7 C₁₆H₁₄F₂N₃O₃P 
• 1408232-37-0 C₂₀H₂₂F₂N₃O₃P 
• 174678-80-9 diethyl [(4-α-bromomethyl)phenyldifluoromethyl]-phosphonate 
• 1386395-63-6 ((2-(hydroxy(methyl)amino)-2-oxoethoxy)(p-tolyl)methyl)phosphonic acid 
• 1386395-56-7 dibenzyl ((2-((benzyloxy)amino)-2-oxoethoxy)(p-tolyl)methyl)phosphonate 
• 1386395-53-4 diethyl ((2-((benzyloxy)amino)-2-oxoethoxy)(p-tolyl)methyl)phosphonate 

Relevant articles and documents

A convenient and mild protocol for preparation of α – trimethylsilyloxyphosphonates using sulfamic acid and their oxidation to α – ketophosphonates in the presence of N-bromosuccinimide

A convenient and mild protocol was developed for the trimethylsilylation of α-hydroxyphosphonates using hexamethyldisilazane as the silylating agent in the presence of sulfamic acid (SA) as a heterogeneous solid acid catalyst in dichloromethane as the rea

CeCl3?7H2O-catalysed hydrophosphonylation of aldehydes and ketones: An expeditious route to α-hydroxyphosphonates under solvent-free conditions

A cerium(III) chloride-catalysed expeditious synthesis of α-hydroxyphosphonates via a modified Abramov synthetic protocol has been developed. The scope of the current protocol is broad, with a range of aromatic, α,β-unsaturated and heterocyclic aldehydes

Bi(NO3)3.5H2O catalyzed phosphonylation of aldehydes: An efficient route to α-hydroxyphosphonates

The Bi(NO3)3.5H2O mediated synthesis of α-hydroxyphosphonates via phosphonylation of aldehydes is reported herein. Both conventional and microwave technology was efficiently applied to range of aromatic, heteroaromatic, α,