1486-28-8

  • Product Name:Diphenylphosphinomethane
  • Molecular Formula:C13H13P
  • Purity:99%
  • Molecular Weight:200.22
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Product Details;

CasNo: 1486-28-8

Molecular Formula: C13H13P

Appearance: Colorless to light yellow liquid

factory and supplier 1486-28-8 Diphenylphosphinomethane in stock

  • Molecular Formula:C13H13P
  • Molecular Weight:200.22
  • Appearance/Colour:Colorless to light yellow liquid 
  • Vapor Pressure:0.00127mmHg at 25°C 
  • Melting Point:117-118 °C 
  • Refractive Index:n20/D 1.625(lit.)  
  • Boiling Point:308.1 °C at 760 mmHg 
  • Flash Point:128.4 °C 
  • PSA:13.59000 
  • Density:1.076 g/mL at 25 °C(lit.)  
  • LogP:2.74910 

Methyldiphenylphosphine(Cas 1486-28-8) Usage

General Description

Methyldiphenylphosphine (PPh2Me) is a monodentate phosphine ligand used in the synthesis of cycloplatinated(II) complexes, where it replaces dimethyl sulfoxide (DMSO) in [PtMe(Vpy)(DMSO)] to form [PtMe(Vpy)(PPh2Me)]. This complex exhibits intense phosphorescence emission in both solid state and solution, attributed to a mixed 3ILCT/3MLCT excited state, and undergoes oxidative addition reactions with alkyl halides via an SN2 mechanism, demonstrating its utility in optoelectronic and catalytic applications.

InChI:InChI=1/C13H13P/c1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13/h2-11H,1H3

1486-28-8 Relevant articles

Br?nsted Acid Promoted Reduction of Tertiary Phosphine Oxides

Krachko, Tetiana,Lyaskovskyy, Volodymyr,Lutz, Martin,Lammertsma, Koop,Slootweg, J. Chris

, p. 916 - 921 (2017)

Recently, Br?nsted acids, such as phosph...

-

Seyferth,Burlitch

, p. 2463 (1963)

-

Ethylene Tetramerization Catalysis: Effects of Aluminum-Induced Isomerization of PNP to PPN Ligands

Lifschitz, Alejo M.,Hirscher, Nathanael A.,Lee, Heui Beom,Buss, Joshua A.,Agapie, Theodor

, p. 1640 - 1648 (2017)

Diphosphinoamines (PNP) are commonly use...

Palladium-Catalyzed Cleavage of P-C Bonds In Quaternary Phosphonium Salts and Its Applications to Organic Synthesis

Sakamoto, Masato,Shimizu, Isao,Yamamoto, Akio

, p. 1101 - 1102 (1995)

Phosphonium salts, PPh4I and PMePh3I, ox...

-

Eyles,Trippett

, p. 67,69 (1966)

-

Dimethylsulfonium methylide in methylation of silylphosphines

Veits,Chuchuryukin,Neganova

, p. 1790 - 1792 (2002)

Selective monodesilylation of bissilylat...

Alane - A novel way to reduce phosphine oxides

Griffin, Sara,Heath, Lucy,Wyatt, Paul

, p. 4405 - 4406 (1998)

Phosphine oxides may be reduced to phosp...

Preparation and properties of a series of structurally diverse aluminium hydrides supported by β-diketiminate and bis(amide) ligands

Nako, Adi E.,Gates, Sarah J.,White, Andrew J.P.,Crimmin, Mark R.

, p. 15199 - 15206 (2013)

The synthesis of a diverse series of hyd...

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...

The Trityl-Cation Mediated Phosphine Oxides Reduction

Landais, Yannick,Laye, Claire,Lusseau, Jonathan,Robert, Frédéric

supporting information, p. 3035 - 3043 (2021/05/10)

Reduction of phosphine oxides into the c...

Reversing Lewis acidity from bismuth to antimony

Balasubramaniam, Selvakumar,Jemmis, Eluvathingal D.,Kumar, Sandeep,Sharma, Deepti,Venugopal, Ajay

supporting information, p. 8889 - 8892 (2021/09/10)

Investigations on the boundaries between...

Reductive conversion of phosphoryl P(O) compounds to trivalent organophosphines R3P

Zhang, Jian-Qiu,Han, Li-Biao

, (2021/02/20)

By introducing trimethylsilyl chloride (...

1486-28-8 Process route

piperazine-1,4-diylbis(diphenylphosphine)oxide

piperazine-1,4-diylbis(diphenylphosphine)oxide

3-ethyl-1H-pyrrole
1551-16-2

3-ethyl-1H-pyrrole

2-Methylpyrazine
109-08-0

2-Methylpyrazine

4,4'-bipyridine
553-26-4

4,4'-bipyridine

2-methylimidazole
693-98-1

2-methylimidazole

trans-2-Butene
624-64-6

trans-2-Butene

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

N-methylaniline
100-61-8

N-methylaniline

diphenylphosphane
829-85-6

diphenylphosphane

diphenyl(methyl)phosphine
1486-28-8

diphenyl(methyl)phosphine

bis(diphenylphosphino)amine
17157-61-8

bis(diphenylphosphino)amine

Conditions
Conditions Yield
at 600 ℃;
2-phenoxyphenyldiphenylphosphine
183383-68-8

2-phenoxyphenyldiphenylphosphine

methyllithium
917-54-4

methyllithium

10-phenyl-10H-phenoxaphosphinine
1225-16-7

10-phenyl-10H-phenoxaphosphinine

10-methyl-10H-phenoxaphosphine
22472-42-0

10-methyl-10H-phenoxaphosphine

triphenylphosphine
603-35-0

triphenylphosphine

diphenyl(methyl)phosphine
1486-28-8

diphenyl(methyl)phosphine

Conditions
Conditions Yield
With water; Multistep reaction;
Product distribution; reactions of tertiary phosphine derivatives of diphenyl ether with lithium reagents; possible mechanism;

1486-28-8 Upstream products

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    60-29-7

    diethyl ether

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    124-41-4

    sodium methylate

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    chloro-diphenylphosphine

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    544-97-8

    dimethyl zinc(II)

1486-28-8 Downstream products

  • 1661-08-1
    1661-08-1

    diphenylethylmethylphosphonium iodide

  • 106141-00-8
    106141-00-8

    methylallyldiphenylphosphonium bromide

  • 1017-88-5
    1017-88-5

    dimethyldiphenylphosphonium iodide

  • 2129-89-7
    2129-89-7

    diphenyl(methyl)phosphine oxide

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