DIPHENYL(P-TOLYL)PHOSPHINE

DIPHENYL(P-TOLYL)PHOSPHINE
  • CAS No.:1031-93-2
Other grades of this product :
DIPHENYL(P-TOLYL)PHOSPHINE Basic information
Product Name:DIPHENYL(P-TOLYL)PHOSPHINE
Synonyms:1-[5-chloro-2-[4-chloro-2-[[(3,4-dichloroanilino)-oxomethyl]amino]phenoxy]phenyl]-3-(3,4-dichlorophenyl)urea;P-TOLYLDIPHENYLPHOSPHINE;Phosphine, (4-methylphenyl)diphenyl-;DIPHENYL(P-TOLYL)PHOSPHINE;DIPHENYL-4-TOLYLPHOSPHINE;DIPHENYL-4-METHYLPHENYLPHOSPHINE;p-Tolyldiphenylphosphine,min.96%;p-Tolyldiphenylphosphine, 96+%
CAS:1031-93-2
MF:C19H17P
MW:276.31
EINECS:213-848-3
Product Categories:Achiral Phosphine;Aryl Phosphine;Ligand;Catalysis and Inorganic Chemistry;Phosphine Ligands;organophosphorus ligand;Phosphorus Compounds
Mol File:1031-93-2.mol
DIPHENYL(P-TOLYL)PHOSPHINE Chemical Properties
Melting point 66-68 °C (lit.)
Boiling point 250 °C(Press: 14 Torr)
storage temp. 2-8°C
form crystal
color white
BRN 646709
CAS DataBase Reference1031-93-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-38-37-36
Safety Statements 26-37/39-39-37
WGK Germany 3
PackingGroup III
HS Code 29319090
MSDS Information
ProviderLanguage
ACROS English
SigmaAldrich English
ALFA English
DIPHENYL(P-TOLYL)PHOSPHINE Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
UsesReactant for:
  • Three-component cyclization
  • Probing coordination ability via a palladium pincer complex
  • Chelation-assisted hydroacylation of olefins with primary alcohols
Reactant for synthesis of:
  • Trinuclear ruthenium carbonyl triarylphosphine cluster complexes
  • Leishmanicidal leads targeting mitochondria through inhibition of the respiratory complex
  • InP nanofibers / metal phosphide nanostructures
  • Peroxyl radical cations via pulse radiolysis one-electron oxidations
Synthesis Reference(s)The Journal of Organic Chemistry, 52, p. 748, 1987 DOI: 10.1021/jo00381a008
DIPHENYL(P-TOLYL)PHOSPHINE Preparation Products And Raw materials

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