161265-03-8

  • Product Name4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene
  • Molecular FormulaC39H32OP2
  • Molecular Weight578.6
  • Purity99%
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Product Details

Quick Details

  • CasNo: 161265-03-8
  • Molecular Formula: C39H32OP2
  • Purity: 99%

Wholesale High Purity 4,5-Bis(diphenylphosphino)-9,9-dimethyl-xanthene 161265-03-8

  • Molecular Formula:C39H32OP2
  • Molecular Weight:578.63
  • Appearance/Colour:white to light yellow crystals 
  • Vapor Pressure:7.61E-17mmHg at 25°C 
  • Melting Point:224-228 °C(lit.) 
  • Boiling Point:665.7 °C at 760 mmHg 
  • Flash Point:449.9 °C 
  • PSA:36.41000 
  • LogP:7.63460 

4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene(Cas 161265-03-8) Usage

Application

4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene is an organophosphorus compound derived from the heterocycle xanthene. It is used as a bidentate ligand and is noteworthy for having a particularly wide bite angle. Such ligands are useful in the hydroformylation of alkenes.

Chemical Properties

White to light yellow crystals

Uses

suzuki reaction

Reactions

Ligand used for the hydroformylation of alkenes. Ligand used in the intermolecular coupling of amides and hydrazones with aryl halides. Ligand used in the intermolecular coupling of amides with aryl halides or triflates. Ligand used in the coupling of heteroarylamines and aryl halides. Ligand used in the hydrophosphinylation of alkenes and alkynes. Ligand used for the Au(I)-catalyzed dehydrogenative silation of alcohols. Ligand used for the sulfinylation of aryl iodides. Ligand used for the Pd-catalyzed carbonylation reaction of aryl bromides and amines. Ligand used for the Ni-cataltzed alkynylcyanation of alkynes. Ligand used for the Pd-catalyzed N-arylation of 3-amino-1H-pyrazole. Ligand used for the Rh-catalyzed dehydrogenation borylation of cyclic alkenes. Ligand used for the Pd-catalyzed intermolecular coupling of H-Phosphonate diesters with benzyl halides. Ligand used for the Pd-catalyzed one pot synthesis of 4-aryl-1H-1,2,3-triazoles. Ligand used for the Pd-catalyzed intermolecular addition of formamides to alkynes. Ligand used for the Pd-catalyzed decarboxylative couplings of 2-(2-azaaryl)acetates with aryl halides and triflates. Ligand used for the Pd-catalyzed benzylic arylation of 2-methyl azaarenes Ligand used for the Pd-catalyzed α-arylation of heteroaromatic ketones. Ligand used for the Pd-catalyzed direct alkynlation of both azoles and azolines. Ligand used for the Cu-catalyzed intermolecular coupling of alkynes with aryl iodides. Ligand used for the Pd-catalyzed ene-type reaction of aldehydes with 1,3-diene. Ligand used for the Ru-catalyzed intermolecular addition of 2-phenylbenzoic acid onto unactivated olefins. Ligand used for the Pd/Cu-catalyzed direct arylation of heteroarenes. Ligand used for the Pd-catalyzed reaction of propargyl-substituted malonate esters with aryl halides. Ligand used for the Pd-catalyzed decarboxylative coupling of tertiary cyanoacetate salts with aryl halides and triflates. Ligand used for the Pd-catalyzed hydroesterification of alkynes. Ligand used for the Cu-catalyzed arylation of arylboronic acids with aldehydes. Ligand used for the Ru-catalyzed oxidative synthesis of heterocycles from alcohols. Ligand used for the Rh-catalyzed borylation of nitriles. Ligand used in the Pd-catalyzed α-arylation of benzylic phosphine oxides. Ligand used in the Pd-Catalyzed Oxidative Coupling of Enamides and Alkynes. Ligand used in the Pd-catalyzed difunctionalization of enol ethers to amino acetals with aminals and alcohols. Ligand used in the Pd-catalyzed alkoxycarbonylation of α-chloroketones.

InChI:InChI=1/C39H32OP2/c1-39(2)33-25-15-27-35(41(29-17-7-3-8-18-29)30-19-9-4-10-20-30)37(33)40-38-34(39)26-16-28-36(38)42(31-21-11-5-12-22-31)32-23-13-6-14-24-32/h3-28H,1-2H3

161265-03-8 Relevant articles

Xanthene-based phosphine oxide host with the planar multi-insulating structure for efficient electrophosphorescence

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, p. 561 - 569 (2012)

A phosphine oxide (PO) host containing p...

Bidentate Phosphines of Heteroarenes: 9,9-Dimethyl-4,5-bis(diphenylphosphino)xanthene

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, p. 75 - 78 (1995)

Twofold lithiation of 9,9-dimethylxanthe...

A new series of tetrahedral Co(II) complexes [CoLX2] (X = NCS, Cl, Br, I) manifesting single-ion magnet features

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In this work we show, using the example ...

Novel phosphine oxide bidentate neutral manganese complex as well as preparation method and application thereof

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Paragraph 0032-0040, (2021/04/26)

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Paragraph 0005; 0008-0009, (2019/07/10)

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161265-03-8 Process route

9,9-dimethyl-4,6-bis(diphenyloxyphosphino)xanthene

9,9-dimethyl-4,6-bis(diphenyloxyphosphino)xanthene

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene
161265-03-8

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene

Conditions
Conditions Yield
With tributylphosphine; iodine; In tetrahydrofuran; acetonitrile; at 20 ℃; for 0.166667h; Inert atmosphere;
95%
acetone
67-64-1

acetone

bis[2-(diphenylphosphino)phenyl] ether
166330-10-5

bis[2-(diphenylphosphino)phenyl] ether

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene
161265-03-8

4,5-bis(diphenylphosphino)-9,9-dimethylxanthene

Conditions
Conditions Yield
With trifluorormethanesulfonic acid; In toluene; at 200 ℃; for 16h; Temperature; Inert atmosphere;
95%

161265-03-8 Upstream products

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    19814-75-6

    9,9-dimethylxanthene

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    808142-24-7

    1,1'-(9,9-dimethyl-9H-xanthene-4,5-diyl)bis-1,1-diphenylphosphine oxide

  • 67-64-1
    67-64-1

    acetone

161265-03-8 Downstream products

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    227805-75-6

    2-(3',5'-dimethylphenylamino)pyridine

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    4300-33-8

    N-(4-methylphenyl)-N'-phenylurea

  • 102-07-8
    102-07-8

    bis(diphenyl)urea

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