134891-99-9

Basic information

• Product Name: Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester
• CAS NO: 134891-99-9
• Molecular Formula: C11H19O4P
• Molecular Weight: 246.243
• Mol File: 134891-99-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester(134891-99-9)
• EPA Substance Registry System: Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester(134891-99-9)

Safety Data

• Hazardous Substances Data: 134891-99-9(Hazardous Substances Data)

Usage

General Description

Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester is a chemical compound with the molecular formula C13H21O5P. It is an ester of phosphonic acid and is commonly used in the synthesis of pharmaceuticals and agrochemicals. Phosphonic acid, [(3-oxo-1-cyclohexen-1-yl)methyl]-, diethyl ester has been found to have potential antioxidant and anti-inflammatory properties, making it a promising candidate for the development of new drugs. Additionally, it has been studied for its potential use in metal chelation therapy, which could be beneficial in the treatment of heavy metal poisoning. However, further research is needed to fully understand its properties and potential applications.

Upstream product

• 16807-60-6 3-methoxycyclohex-2-en-1-one 
• 683-08-9 Diethyl methylphosphonate 
• 5323-87-5 3-Ethoxycyclohex-2-en-1-one 
• 818-38-2 Diethyl glutarate 
• 5682-75-7 3-chloro-2-cyclohexenone 
• 84978-80-3 2-(phenylsulfinyl)cyclohex-2-en-1-one 
• 173171-39-6 diethyl <(1-hydroxy-3-chloro-2-cyclohexen-1-yl)methyl>phosphonate 
• 153983-68-7 [7-(Diethoxy-phosphoryl)-2,6-dioxo-heptyl]-phosphonic acid diethyl ester 
• 134891-93-3 <(1-hydroxy-2-cyclohexen-1-yl)methyl>phosphonate 
• 23740-61-6 2-(phenylsulfanyl)-2-cyclohexanone 
• 67502-51-6 diethyl [(phenylselanyl)methyl]phosphonate 
• 930-68-7 cyclohexenone 

Downstream Products

• 1096156-00-1 3-(4-(diphenylamino)styryl)cyclohex-2-enone 
• 209402-40-4 diethyl (3-oximinocyclohex-1-enyl)methylphosphonate 
• 60815-18-1 diethyl [(3-methoxyphenyl)methyl]phosphonate 
• 29179-03-1 (E)-3-(prop-1-en-1-yl)cyclohex-2-en-1-one 

Relevant articles and documents

A General Approach to 3-Phosphorylmethyl Cycloalkenones by Intramolecular Horner-Wittig Reaction of Bis-β-ketophosphonates

The reaction of dicarboxylic acid diesters with lithiomethylphosphonates was found to give bis-β-keto phosphonates 1 2(CH2)n (n = 2, 3, 4), a new class of compounds.Their cyclization under basic conditions provides an easy access to five

Synthesis of 3-(phosphorylmethyl)cycloalkenones by forced conjugate addition of α-phosphonate carbanions to cyclic enones

Cycloalkenones were found to react with α-lithiated diethyl (phenylselanyl)methylphosphonate preferentially or exclusively at the carbonyl group giving 1,2-adducts. When complexes of cycloalkenones with aluminum tris(2,6-diphenylphenoxide) were used for t

Oxidative rearrangement of phosphorus containing tertiary allylic alcohols: Synthesis of (3-oxo-1-cycloalkenyl)phosphonates, -methylphosphonates, -methyldiphenylphosphine oxides and their epoxy derivatives

Regioselective 1,2-addition of dimethylphosphite, diethyl (lithiomethyl)phosphonate, or (lithiomethyl)diphenylphosphine oxide to 2-cyclopenten-1-one (1a) or 2-cyclohexen-1-one (1b) affords the corresponding phosphorus containing, tertiary allylic alcohols