210691-22-8

Basic information

• Product Name: (diallyl ether)(triphenylphosphane)palladium⁽⁰⁾
• Synonyms: (diallyl ether)(triphenylphosphane)palladium⁽⁰⁾
• CAS NO: 210691-22-8
• Molecular Weight: 466.856
• Mol File: 210691-22-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (diallyl ether)(triphenylphosphane)palladium⁽⁰⁾(CAS DataBase Reference)
• NIST Chemistry Reference: (diallyl ether)(triphenylphosphane)palladium⁽⁰⁾(210691-22-8)
• EPA Substance Registry System: (diallyl ether)(triphenylphosphane)palladium⁽⁰⁾(210691-22-8)

Safety Data

• Hazardous Substances Data: 210691-22-8(Hazardous Substances Data)

Upstream product

• 557-40-4 Allyl ether 
• 14221-01-3 tetrakis(triphenylphosphine) palladium⁽⁰⁾ 
• 12107-56-1 dichloro(cycloocta-1,5-diene)palladium (II) 
• 210691-06-8 (μ-η(2),η(2)-C7H12)[Pd(η(2),η(2)-C7H12)]2 
• 210691-15-9 (C6H5)3PPd(η(2),η(2)-C7H12) 
• 210691-07-9 (μ-η(2),η(2)-C6H10O)(Pd(η(2),η(2)-C6H10O))2 
• 603-35-0 triphenylphosphine 
• 31989-57-8 bis(triphenylphosphine)palladium⁽⁰⁾ 

Downstream Products

• 292177-02-7 Pd((C₆H₅)3P)(C₈H₁₂) 

Relevant articles and documents

Molecularly defined palladium(0) monophosphine complexes as catalysts for efficient cross-coupling of aryl chlorides and phenylboronic acid

Various 1,6-diene palladium(0) monophosphine complexes have been prepared from tmedaPd(CH3)2, PR3, and the corresponding 1,6-diene. These molecularly defined Pd complexes catalyzed the Suzuki coupling of aryl chlorides wit

Hepta-1,6-diene and diallyl ether complexes of palladium(0) and platinum(0): A route to L-M(alkene)2 complexes containing non-activated alkenes

With hepta-1,6-diene and diallyl ether, Pd0 and Pt0 form highly reactive homoleptic dinuclear M2(1,6-diene)3 complexes, which are cleaved by donors L (e.g. C2H4, phosphanes, phosphites, isonitriles) to afford mononuclear derivatives L-M(1,6-diene); the X-ray structure of (Me3P)Pd{(η2-CH2=CHCH2) 2O} has been determined.