1641-61-8

Basic information

• Product Name: DIMETHYL CYCLOHEXYLPHOSPHONATE
• Synonyms: DIMETHYL CYCLOHEXYLPHOSPHONATE;Dimethyl cyclohexanephosphonate;P-Cyclohexylphosphonic acid dimethyl ester
• CAS NO: 1641-61-8
• Molecular Formula: C₈H₁₇O₃P
• Molecular Weight: 192.19
• Mol File: 1641-61-8.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 30-32°C/0.1mm
• Flash Point: 30-32°C/0.1mm
• Appearance: /Liquid
• Density: 1.05
• Vapor Pressure: 0.02mmHg at 25°C
• Refractive Index: 1.434
• CAS DataBase Reference: DIMETHYL CYCLOHEXYLPHOSPHONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL CYCLOHEXYLPHOSPHONATE(1641-61-8)
• EPA Substance Registry System: DIMETHYL CYCLOHEXYLPHOSPHONATE(1641-61-8)

Safety Data

• Hazardous Substances Data: 1641-61-8(Hazardous Substances Data)

Usage

General Description

DIMETHYL CYCLOHEXYLPHOSPHONATE is an organic chemical compound known for its use in a wide range of applications in various industries. It is part of the organophosphorus compounds class, primarily distinguished by the presence of a phosphorus atom in its molecular structure. It has the chemical formula C8H17O3P, signifying the presence of carbon, hydrogen, oxygen, and phosphorus atoms in its structure. Key characteristics include its clear colorless liquid appearance, having a strong odor, and its soluble properties. Due to its unique chemical nature, it is typically used in the production of flame retardants, plasticizers, and insecticides. It is important to handle this chemical 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 
• 286-20-4 cyclohexane-1,2-epoxide 
• 868-85-9 Dimethyl phosphite 
• 2240-41-7 dimethyl phenylphosphonate 
• 4545-18-0 N'-cyclohexylidene-4-methylbenzene-1-sulfonohydrazide 
• 3855-24-1 cyclohexane-1,1-dithiol 
• 110-83-8 cyclohexene 
• 63007-12-5 C₁₅H₂₅N₂O₅PS 

Downstream Products

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

Relevant articles and documents

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

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.