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Tris(2-Methoxyphenyl)phosphine

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Tris(2-Methoxyphenyl)phosphine Basic information

Product Name:
Tris(2-Methoxyphenyl)phosphine
Synonyms:
  • Phosphine, tris(2-methoxyphenyl)-
  • Tris(2-methoxyphenyl)phosphine,98%
  • TRI(2-METHOXYPHENYL)PHOSPHINE
  • TRIS(O-ANISYL)PHOSPHINE
  • TRIS(2-METHOXYPHENYL)PHOSPHINE
  • TRIS(O-METHOXYPHENYL)PHOSPHINE
  • Tri(o-anisyl)phosphine
  • TRIS-(2-ANISYL)PHOSPHINE
CAS:
4731-65-1
MF:
C21H21O3P
MW:
352.36
EINECS:
225-235-8
Product Categories:
  • Achiral Phosphine
  • Aryl Phosphine
  • organophosphine ligand
Mol File:
4731-65-1.mol
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Tris(2-Methoxyphenyl)phosphine Chemical Properties

Melting point:
204-208 °C
Boiling point:
477.3±40.0 °C(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
form 
Liquid
color 
Colorless to yellow or pale orange
Water Solubility 
Slightly soluble in water.
Sensitive 
Air Sensitive
BRN 
2776186
InChI
InChI=1S/C21H21O3P/c1-22-16-10-4-7-13-19(16)25(20-14-8-5-11-17(20)23-2)21-15-9-6-12-18(21)24-3/h4-15H,1-3H3
InChIKey
IIOSDXGZLBPOHD-UHFFFAOYSA-N
SMILES
P(C1=CC=CC=C1OC)(C1=CC=CC=C1OC)C1=CC=CC=C1OC
CAS DataBase Reference
4731-65-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26
WGK Germany 
3
TSCA 
No
HS Code 
29319090

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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Tris(2-Methoxyphenyl)phosphine Usage And Synthesis

Chemical Properties

white powder or crystals

Uses

suzuki reaction

Uses

Tris(2-methoxyphenyl)phosphine is a phosphine ligand used for catalysis. It is used as a catalyst for allylic substitution of simple alkenes, suzuki coupling reactions, hydrogenation of quinolines and other addition reactions.

References

[1] Raymond C. Bott, Graham Smith, Peter C. Healy. “Structural studies of two-coordinate complexes of tris(2-methoxylphenyl)phosphine and tris(4-methoxyphenyl)phosphine with gold(I) halides.” Polyhedron 26 12 (2007): Pages 2803-2809.
[2] O. Shawkataly. “Pentacarbonyl[tris(2-methoxyphenyl)phosphine-P]chromium and its Molybdenum Analogue.” Acta crystallographica. Section C, Crystal structure communications 75 1 (1996): 1352–1355.

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