1641-61-8

Usage

Uses

Used in Chemical Industry:
DIMETHYL CYCLOHEXYLPHOSPHONATE is used as a raw material for the production of flame retardants, which are essential in preventing the spread of fire in various materials and products.
Used in Plastics Industry:
DIMETHYL CYCLOHEXYLPHOSPHONATE is used as a plasticizer, enhancing the flexibility and workability of plastics by reducing their rigidity and brittleness.
Used in Agricultural Industry:
DIMETHYL CYCLOHEXYLPHOSPHONATE is used as an ingredient in the formulation of insecticides, helping to control pests and protect crops from damage.
It is important to handle DIMETHYL CYCLOHEXYLPHOSPHONATE with care due to its toxicity and potential ecological impacts when mishandled.

InChI:InChI=1/C8H17O3P/c1-10-12(9,11-2)8-6-4-3-5-7-8/h8H,3-7H2,1-2H3

Upstream product

• 124-41-4 sodium methylate 
• 1005-22-7 cyclohexylphosphonic dichloride 
• 55499-38-2 (1-Methylsulfanyl-cyclohexyl)-phosphonic acid dimethyl ester 
• 63007-12-5 C₁₅H₂₅N₂O₅PS 
• 110-83-8 cyclohexene 
• 868-85-9 Dimethyl phosphite 
• 286-20-4 cyclohexane-1,2-epoxide 
• 3855-24-1 cyclohexane-1,1-dithiol 
• 4545-18-0 N'-cyclohexylidene-4-methylbenzene-1-sulfonohydrazide 
• 2240-41-7 dimethyl phenylphosphonate 

Downstream Products

• 19236-53-4 Cyclohexylphosphonsaeure-monomethylester 
• 10184-64-2 dimethyl 1-hydroxycyclohexylphosphonate 

Relevant academic research and scientific papers

Reactions of dialkyl phosphonates with hexacarbonylmolybdenum(0) and hexacarbonyltungsten(0). Structure of intermediates in the catalytic phosphorylation of alkenes

Reactions of dialkyl phosphonates with catalytic precursors in the phosphorylation of alkenes and aryl halides, homoligand molybdenum(0) and tungsten(0) carbonyl complexes, were studied by quantum-chemical and spectroscopic (IR and NMR) methods. Schemes w

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

Mild and Selective Rhodium-Catalyzed Transfer Hydrogenation of Functionalized Arenes

Diboron-mediated rhodium-catalyzed transfer hydrogenation of functionalized arenes is reported. In addition to good functional group tolerance, the reaction features operational simplicity and controllable chemoselectivity. The general applicability of this procedure is demonstrated by the selective hydrogenation of a range of arenes, including functionalized benzenes, biphenyls, and polyaromatics.

Probing the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under free-radical conditions

Hydrophosphonylation is an efficient process to create carbon-phosphorus bonds from unsaturated C-C bonds and to give rise to alkylphosphonate or vinylphosphonate derivatives. In this work, we report on the reactivity of H-phosphonate derivatives for the hydrophosphonylation of various alkenes and alkynes under photoinduced free-radical conditions. The reaction was carried out on activated, unactivated and/or disubstituted alkenes or alkynes with 2,2-dimethoxy-2-phenylacetophenone as a photoinitiator under UV irradiation.

Microwave catalyzed reactions of H-dimethylphosphonate with oxiranes

Microwave catalyzed reactions of H-dimethylphosphonate with 1,2-epoxydecane, 5,6-epoxy-1-hexene, 1,2-epoxybutane and cyclohexene oxide have been found to cause oxirane ring opening, deoxygenation and hydrophosphorylation. 1,2-Epoxydecane gave three pairs