3808-22-8

Basic information

• Product Name: Phosphonic acid dicyclohexyl ester
• Synonyms: Phosphonic acid dicyclohexyl ester
• CAS NO: 3808-22-8
• Molecular Formula: C₁₂H₂₃O₃P
• Molecular Weight: 245.275041
• Mol File: 3808-22-8.mol
• Article Data: 9

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: g/cm³
• CAS DataBase Reference: Phosphonic acid dicyclohexyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Phosphonic acid dicyclohexyl ester(3808-22-8)
• EPA Substance Registry System: Phosphonic acid dicyclohexyl ester(3808-22-8)

Safety Data

• Hazardous Substances Data: 3808-22-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H22O3P/c13-16(14-11-7-3-1-4-8-11)15-12-9-5-2-6-10-12/h11-12H,1-10H2/q+1

Upstream product

• 762-04-9 phosphonic acid diethyl ester 
• 108-93-0 cyclohexanol 
• 868-85-9 Dimethyl phosphite 
• 2310-48-7 monocyclohexyl phosphite 
• 615-43-0 2-iodophenylamine 
• 100-52-7 benzaldehyde 
• 676329-47-8 cyclohexyl hypophosphite 
• 3959-05-5 2-bromobenzylamine 

Downstream Products

• 80986-94-3 di-cyclohexyl 2-oxo-4-oxetanylmethylphosphonate 
• 84350-97-0 1,2-dihydroxy-1,2-bis(dicyclohexyloxyphosphinyl)ethane 
• 51672-37-8 dicyclohexyl phosphorochloridate 
• 1385877-57-5 dicyclohexyl trifluoromethylphosphonate 
• 1623-23-0 dicyclohexyl hydrogen phosphate 
• 1362708-18-6 C₁₃H₂₂F₃O₄P 

Relevant articles and documents

Way to Enforce Selectivity via Steric Hindrance: Improvement of Am(III)/Eu(III) Solvent Extraction by Loaded Diphosphonic Acid Esters

Hybrid donor extractants are a promising class of compounds for the separation of trivalent actinides and lanthanides. Here, we investigated a series of sterically loaded diphosphonate ligands based on bipyridine (BiPy-PO-iPr and BiPy-PO-cHex) and phenant

Synthesis and extraction behavior of alkyl and cyclic aminophosphonates towards actinides

Alkyl and cyclic substituted aminophosphonates (AmPs) were synthesized and characterized with various spectroscopic techniques. The molecular structures of diphenyl phenyl aminophosphonate (DPhPhAmP) and diphenyl cyclohexyl aminophosphonate (DPhCyAmP) wer

Phosphorus-carbon bond formation: Palladium-catalyzed cross-coupling of H-phosphinates and other P(O)H-containing compounds

Two generally applicable systems have been developed for the cross-coupling of P(O)H compounds with Csp2-X and related partners. Palladium catalysis using a ligand/additive combination, typically either xantphos/ethylene glycol or 1,1-bis(diphenylphosphino)ferrocene/1,2- dimethoxyethane, with diisopropylethylamine as the base, proved to be generally useful for the synthesis of numerous P-C containing compounds. Routinely, 2 mol% of catalyst are employed (less than half the amount typically employed in most other literature reports). In most cases, excellent results are obtained with a variety of electrophiles (RX, where R=alkenyl, allyl, alkynyl, etc.). The full account of our studies is disclosed, including tandem hydrophosphinylation/ coupling and coupling/coupling for doubly catalytic phosphorus-carbon bond formation. The methodology compares favorably with any existing literature report. The use of an additive appears to be a generally useful strategy to control the reactivity of phosphinylidene compounds. Copyright