Tris(4-methoxyphenyl)phosphine

Tris(4-methoxyphenyl)phosphine
Names
	Preferred IUPAC name Tris(4-methoxyphenyl)phosphane
Identifiers
CAS Number	855-38-9;
3D model (JSmol)	Interactive image;
ChemSpider	63260;
ECHA InfoCard	100.011.567
EC Number	212-723-0;
PubChem CID	70071;
UNII	PF5BT47LZ8 ;
CompTox Dashboard (EPA)	DTXSID3061217 ;
	InChI InChI=1S/C21H21O3P/c1-22-16-4-10-19(11-5-16)25(20-12-6-17(23-2)7-13-20)21-14-8-18(24-3)9-15-21/h4-15H,1-3H3 Key: UYUUAUOYLFIRJG-UHFFFAOYSA-N;
	SMILES COC1=CC=C(C=C1)P(C2=CC=C(C=C2)OC)C3=CC=C(C=C3)OC;
Properties
Chemical formula	P(C6H4OCH3)3
Appearance	white solid
Melting point	131 °C (268 °F; 404 K)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Tris(4-methoxyphenyl)phosphine is the organophosphorus compound with the formula (CH₃OC₆H₄)₃P. Several isomers of this formula are known, but the symmetrical derivative with methoxy groups in the 4-position is most studied. The compound is used as a ligand in organometallic chemistry and homogeneous catalysis.^[1]

^ Evans, D.; Osborn, J. A.; Wilkinson, G. (1968). "Hydroformylation of alkenes by use of rhodium complex catalysts". Journal of the Chemical Society A: Inorganic, Physical, Theoretical: 3133. doi:10.1039/j19680003133.

[1] Evans, D.; Osborn, J. A.; Wilkinson, G. (1968). "Hydroformylation of alkenes by use of rhodium complex catalysts". Journal of the Chemical Society A: Inorganic, Physical, Theoretical: 3133. doi:10.1039/j19680003133.

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