4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE

4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Basic information
Reactions
Product Name:4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE
Synonyms:4,6-Bis(diphenylphosphino)phenoxazine 97%;N-XantPhos 97%;4,6-Bis(diphenylphosphino)phenoxazine, min. 98%;4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE;4,6-Bis(diphenylphosphino)phenoxazine, NIXANTPHOS;4,6-Bis(diphenylphosphino)phenoxazine,min.98%NIXANTPHOS;4,6-Bis(diphenylphosphino)phenoxazine, 98+%;4,6-Bis(diphenylphosphino)phenoxazine, 98+% NIXANTPHOS
CAS:261733-18-0
MF:C36H27NOP2
MW:551.55
EINECS:
Product Categories:Achiral Phosphine;Aryl Phosphine;Phosphine Ligands;Synthetic Organic Chemistry;organophosphine ligand
Mol File:261733-18-0.mol
4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Structure
4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Chemical Properties
Melting point 256-262 °C
Boiling point 662.1±55.0 °C(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka1.34±0.20(Predicted)
form Powder
color white to off-white
Water Solubility Miscible with water.
InChIKeyHSWZLYXRAOXOLL-UHFFFAOYSA-N
CAS DataBase Reference261733-18-0
Safety Information
Risk Statements 36/37/38
Safety Statements 22-24/25
WGK Germany 3
TSCA No
HS Code 2934.99.4400
MSDS Information
ProviderLanguage
SigmaAldrich English
4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Usage And Synthesis
Reactions
  1. A large bite-angle chelating bisphosphine that provides high levels of linear-to-branched selectivity in the hydroformylation of alkenes.
  2. A Deprotonatable Ligand for Room-Temperature Palladium-Catalyzed Cross-Couplings of Aryl Chlorides.
Reactions of 261733-18-0
Uses4,6-Bis(diphenylphosphino)phenoxazine used as an intermediate in the manufacture of pharmaceuticals, agrochemicals, dyestuffs, fine chemicals, medical and material synthesis.
Uses4,6-Bis(Diphenylphosphino)phenoxazine is used as a palladium catalyst in reactions involving the synthesis of triarylmethanes.
UsesN-XantPhos is a deprotonatable chelating aryldiphosphine ligand that can be used in:
  • The preparation of Pd-NiXantphos catalyst system for the room temperature cross-coupling reactions of unactivated aryl chlorides.
  • The synthesis of cinchonine iridium(III) cyclometalated complex that exhibits luminescence and good quantum efficiency.
  • N-XantPhos and N-modified counterparts are also used in the preparation of rhodium based catalysts for hydroformylation reaction.

4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE Preparation Products And Raw materials
1.1'-Binaphthyl-2.2'-diphemyl phosphine 4,6-BIS(DIPHENYLPHOSPHINO)PHENOXAZINE (R)-(2-METHOXYPHENYL)METHYLPHENYLPHOSPHINE (OXYDI-2,1-PHENYLENE)BIS(DIPHENYLPHOSPHINE) P-ANISYLDIPHENYLPHOSPHINE Phenoxazine (S)-(2-METHOXYPHENYL)METHYLPHENYLPHOSPHINE

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