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Methyl(2,4,6-trimethylphenyl)phosphane

Base Information Edit
  • Chemical Name:Methyl(2,4,6-trimethylphenyl)phosphane
  • CAS No.:502966-91-8
  • Molecular Formula:C10H15P
  • Molecular Weight:166.203
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20587308
  • Wikidata:Q82479711
  • Mol file:502966-91-8.mol
Methyl(2,4,6-trimethylphenyl)phosphane

Synonyms:502966-91-8;Methyl(2,4,6-trimethylphenyl)phosphane;SCHEMBL5380061;DTXSID20587308

Suppliers and Price of Methyl(2,4,6-trimethylphenyl)phosphane
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Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of Methyl(2,4,6-trimethylphenyl)phosphane Edit
Chemical Property:
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:1
  • Exact Mass:166.091137476
  • Heavy Atom Count:11
  • Complexity:110
Purity/Quality:
Safty Information:
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  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC(=C(C(=C1)C)PC)C
Technology Process of Methyl(2,4,6-trimethylphenyl)phosphane

There total 1 articles about Methyl(2,4,6-trimethylphenyl)phosphane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
2,4,6-trimethylphenyl bromide; With magnesium; In tetrahydrofuran; at 20 ℃;
methyldichlorophosphane; In tetrahydrofuran; diethyl ether; Heating;
With lithium aluminium tetrahydride; at 20 ℃; for 2.5h; Further stages.;
DOI:10.1021/ja070225a
Guidance literature:
With sodium trimethylsilanolate; dichlorobis(tri-O-tolylphosphine)palladium; In tetrahydrofuran; benzene; for 20h; Heating;
DOI:10.1021/ja070225a
Guidance literature:
With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; byproducts: (DBUH)(BPh4); (N2); using Schlenk techniques; suspending of CpMn(CO)2(CPh)BPh4 in CH2Cl2 at -50°C, addn. of HP(Me)Mes via syringe under stirring, monitoring by IR for 0.5 h, cooling to -80°C, treatment with DBU (1 equiv.), warming to room temp.; removal of solvent under vac., extn. with ether, filtration, evapn. of combined extracts under vac., recrystn. from ether-hexane; elem. anal.;
DOI:10.1021/om2000772
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