7351-26-0

Usage

Uses

Used in Agricultural Chemicals Industry:
Phosphonic acid, cyclohexyl-, bis(1-methylethyl) ester is used as an intermediate in the production of herbicides, insecticides, and fungicides for its ability to enhance the effectiveness and stability of these agricultural chemicals.
Used in Water Treatment Chemicals Industry:
Phosphonic acid, cyclohexyl-, bis(1-methylethyl) ester is utilized as a chelating agent and corrosion inhibitor in water treatment chemicals, preventing the formation of scale and rust in water systems, thereby improving the efficiency and longevity of water infrastructure.
Used in Pharmaceutical Industry:
Phosphonic acid, cyclohexyl-, bis(1-methylethyl) ester is employed in the manufacturing of pharmaceuticals, where its chelating properties can be harnessed to improve drug delivery and stability.
Used in Industrial Products:
Phosphonic acid, cyclohexyl-, bis(1-methylethyl) ester is also used in the production of various industrial products, leveraging its versatility and ability to form stable complexes with metals for applications such as metalworking fluids, coatings, and adhesives.

Upstream product

• 55499-41-7 diisopropyl (1-mercaptocyclohexyl)phosphonate 
• 1809-20-7 diisopropyl hydrogenphosphonate 
• 110-83-8 cyclohexene 
• 111-24-0 1,5-dibromo-pentane 
• 99709-52-1 diisopropyl (iodomethyl)phosphonate 
• 3855-24-1 cyclohexane-1,1-dithiol 
• 116-17-6 triisopropyl phosphite 
• 88020-45-5 (1,1,1-trichloromethyl)phosphonic acid diisopropyl ester 
• 27344-79-2 sodium diisopropyl phosphite 
• 683-60-3 sodium isopropylate 
• 1005-22-7 cyclohexylphosphonic dichloride 

Downstream Products

• 186187-33-7 (1-Azido-cyclohexyl)-phosphonic acid diisopropyl ester 
• 60324-15-4 diisopropyl cyclohex-1-enylphosphonate 
• 60324-04-1 1-Aminocyclohexanphosphonsaeure-di-i-propylester 
• 67398-11-2 α-amino cyclohexylphosphonic acid 
• 7351-28-2 Cyclohexylphosphonsaeure-monoisopropylester 

Relevant academic research and scientific papers

A practical synthesis of cycloalkylphosphonates from trichloromethylphosphonates

Cycloalkylphosphonates 5 with ring size varying from 4 to 6 were synthesized in good overall yields, in two steps from trichloromethylphosphonates and ω-dibromoalkanes, via the corresponding α-trimethylsilyl cycloalkylphosphonates 4.

One-pot and efficient electrosynthesis of cycloalkylphosphonates from diisopropyl trichloromethylphosphonate using magnesium electrochemical activation

Various diisopropyl cycloalkylphosphonates were easily prepared in an one-pot sequence under mild conditions, by electrolysing diisopropyl trichloromethylphosphonate in the presence of ω,ω-dibromoalkanes. The use of an electrochemical activated magnesium anode significantly improved the rate and the yield of the two first steps of the reaction.

Facile solid-phase synthesis of cycloalkylphosphonates and 1-cycloalkenylphosphonates using polymer-supported phenylsulfonylmethylphosphonates

A facile procedure for the solid-phase synthesis of cycloalkylphosphonates and 1-cycloalkenylphosphonates in good yields and high purities using polystyrene-supported phenylsulfonylmethylphosphonates with traceless sulfone linker strategy is described. Copyright Taylor & Francis Group, LLC.

Addition of dialkyl hydrogen phosphites to alkenes in the presence of carbonyl complexes of chromium subgroup metals and iron

Depending on the reactant ratio and order of their mixing, reactions of dialkyl hydrogen phosphite with alkenes in the presence of catalytic amounts of homoligand carbonyl complexes of iron or chromium subgroup metals yield phosphonates by two pathways: r

Free-Radical Phosphorylation of Olefins Initiated by Anodic Oxidation

Electrochemical oxidation of lithium and sodium dialkyl phosphites generates dialkyl phosphonyl radicals, which initiate chain free-radical addition of dialkyl phosphites across the alkene multiple bond to form alkyl(cycloalkyl)phosphonates. Alkyl(cycloalkyl)phosphonates are formed simultaneously owing to anodic oxidation of adsorbed primary radical adducts of phosphonyl radical and alkene molecule to give the carbenium cation, followed by deprotonation of the latter.