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[(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl]palladium(II) chloride_Molecular_structure_CAS_191654-69-0)
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[(R)-(+)-2,2′-Bis(di-p-tolylphosphino)-1,1′-binaphthyl]palladium(II) chloride

Catalog No. 708461 Name Sigma Aldrich
CAS Number 191654-69-0 Website http://www.sigmaaldrich.com
M. F. C48H40Cl2P2Pd Telephone 1-800-521-8956
M. W. 856.104722 Fax
Purity Email
Storage Chembase ID: 142888

SYNONYMS

Title
[(R)-(+)-2,2′-双(二-对甲苯基膦)-1,1′-联萘]氯化钯(II)
IUPAC name
(1-{2-[bis(4-methylphenyl)phosphanyl]naphthalen-1-yl}naphthalen-2-yl)bis(4-methylphenyl)phosphane; dichloropalladium
IUPAC Traditional name
(1-{2-[bis(4-methylphenyl)phosphanyl]naphthalen-1-yl}naphthalen-2-yl)bis(4-methylphenyl)phosphane; palladium chloride
Synonyms
[PdCl2{(R)-4-tolylbinap}]

DATABASE IDS

CAS Number 191654-69-0
MDL Number MFCD11656205

PROPERTIES

Empirical Formula (Hill Notation) C48H40Cl2P2Pd
Melting Point >300 °C
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H302 + H312 + H332-H315-H319-H335
European Hazard Symbols Harmful Harmful (Xn)
MSDS Link Download
Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P280-P305 + P351 + P338
Risk Statements 20/21/22-36/37/38
Safety Statements 26
German water hazard class 3

DETAILS

Description (English)
Packaging
100, 500 mg in glass bottle
Application
Catalyst for:
• Enantioselective preparation of hydroxydicarbonyls via aldol addition of pyruvates and diketones with ketene thioacetal1
• Stereoselective aldol condensation using trimethyl[[(phenyl)ethenyl]oxy]silane and benzaldehyde as reactants2
• Stereoselective preparation of naphthalenols via alkylative ring opening of oxabenzonorbornadienes with dialkylzinc3Reactant for:
• Preparation of palladium bis(diphenylphosphino)binaphthyl aqua mononuclear and hydroxo-bridged dinuclear complexes4
Description (简体中文)
包装
100, 500 mg in glass bottle
Application
Catalyst for:
• Enantioselective preparation of hydroxydicarbonyls via aldol addition of pyruvates and diketones with ketene thioacetal1
• Stereoselective aldol condensation using trimethyl[[(phenyl)ethenyl]oxy]silane and benzaldehyde as reactants2
• Stereoselective preparation of naphthalenols via alkylative ring opening of oxabenzonorbornadienes with dialkylzinc3Reactant for:
• Preparation of palladium bis(diphenylphosphino)binaphthyl aqua mononuclear and hydroxo-bridged dinuclear complexes4

REFERENCES