6372-42-5

  • Product Name:Cyclohexyldiphenylphosphine
  • Molecular Formula:C18H21 P
  • Purity:99%
  • Molecular Weight:268.338
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Product Details;

CasNo: 6372-42-5

Molecular Formula: C18H21 P

Appearance: white to light yellow crystal powder

factory and supplier 6372-42-5 Cyclohexyldiphenylphosphine in stock

  • Molecular Formula:C18H21 P
  • Molecular Weight:268.338
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:1.85E-05mmHg at 25°C 
  • Melting Point:58-62 ºC 
  • Boiling Point:374 °C at 760 mmHg 
  • Flash Point:189.4 °C 
  • PSA:13.59000 
  • LogP:4.45200 

Cyclohexyldiphenylphosphine(Cas 6372-42-5) Usage

InChI:InChI=1/C18H21P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-2,4-7,10-13,18H,3,8-9,14-15H2

6372-42-5 Relevant articles

Synthesis method of phosphine (III) compound

-

Paragraph 0020, (2021/11/27)

The invention aims to provide an aryl ph...

A Lewis Base Nucleofugality Parameter, NFB, and Its Application in an Analysis of MIDA-Boronate Hydrolysis Kinetics

García-Domínguez, Andrés,Gonzalez, Jorge A.,Leach, Andrew G.,Lloyd-Jones, Guy C.,Nichol, Gary S.,Taylor, Nicholas P.

supporting information, (2022/01/04)

The kinetics of quinuclidine displacemen...

Direct and Scalable Electroreduction of Triphenylphosphine Oxide to Triphenylphosphine

Manabe, Shuhei,Sevov, Christo S.,Wong, Curt M.

, p. 3024 - 3031 (2020/03/10)

The direct and scalable electroreduction...

Versatile Visible-Light-Driven Synthesis of Asymmetrical Phosphines and Phosphonium Salts

Arockiam, Percia Beatrice,Lennert, Ulrich,Graf, Christina,Rothfelder, Robin,Scott, Daniel J.,Fischer, Tillmann G.,Zeitler, Kirsten,Wolf, Robert

supporting information, p. 16374 - 16382 (2020/11/03)

Asymmetrically substituted tertiary phos...

6372-42-5 Process route

(cyclohexyl)diphenylphosphane oxide
13689-20-8

(cyclohexyl)diphenylphosphane oxide

cyclohexyldiphenylphosphine
6372-42-5

cyclohexyldiphenylphosphine

Conditions
Conditions Yield
With copper(II) trifluoromethanesulfonate; 1,1,3,3-Tetramethyldisiloxane; In toluene; at 100 ℃; Inert atmosphere;
86%
With oxalyl dichloride; hydrogen; In chloroform-d1; at 130 ℃; for 18h; under 60006 Torr; Reagent/catalyst;
85%
(cyclohexyl)diphenylphosphane oxide; With trifluoroacetic anhydride; In 1,4-dioxane; at 20 ℃; for 0.5h; Inert atmosphere;
With 15-crown-5; sodium hydride; sodium hydrogencarbonate; In 1,4-dioxane; at 150 ℃; for 24h; Inert atmosphere;
85%
With copper(II) bis(trifluoromethanesulfonate); 1,1,3,3-tetramethyldisilazane; In toluene; at 80 ℃;
82%
With copper(II) bis(trifluoromethanesulfonate); 1,1,3,3-tetramethyldisilazane; In toluene; at 80 ℃;
82%
With triphenyl phosphite; diphenyl hydrogen phosphite; iodine; In tetrahydrofuran; at 20 ℃; Inert atmosphere;
75%
With oxalyl dichloride; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; triethylamine; In dichloromethane; at 40 ℃; for 2h; Inert atmosphere;
73%
With diethoxymethylane; Bis(p-nitrophenyl) phosphate; In toluene; at 110 ℃; chemoselective reaction; Inert atmosphere;
70%
With aluminum (III) chloride; N,N,N,N,-tetramethylethylenediamine; tetrabutyl-ammonium chloride; tert-butylammonium hexafluorophosphate(V); In acetonitrile; at -20 ℃; Inert atmosphere; Glovebox; Electrolysis;
45%
(cyclohexyl)diphenylphosphane oxide; With [Fe(CO)(1,3-bis(diphenylphosphino)propane)H(NO)]; phenylsilane; N-ethyl-N,N-diisopropylamine; In toluene; at 100 ℃; for 18h; Schlenk technique;
With sodium hydroxide; In methanol; water; toluene; at 20 ℃; for 1h; chemoselective reaction; Schlenk technique;
44%
With indium(III) bromide; 1,1,3,3-Tetramethyldisiloxane; In toluene; at 100 ℃; for 22h; Inert atmosphere; Sealed tube;
chloro-diphenylphosphine
1079-66-9,74391-44-9

chloro-diphenylphosphine

1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate
126812-30-4

1,3-dioxoisoindolin-2-yl cyclohexanecarboxylate

cyclohexyldiphenylphosphine
6372-42-5

cyclohexyldiphenylphosphine

Conditions
Conditions Yield
With N,N,N',N'',N'''-pentamethyldiethylenetriamine; zinc; In N,N-dimethyl-formamide; at 20 ℃; for 12h; Reagent/catalyst; Time;
95%

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