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811862-77-8

811862-77-8 Structure

811862-77-8 Structure
IdentificationBack Directory
[Name]

BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
[CAS]

811862-77-8
[Synonyms]

palladium(0)
Bis(3,5,3',5′-diMethoxydibenz
Bis(3,5,3',5'-dimethoxydibenzyL
BIS(3 5 3' 5'-DIMETHOXYDIBENZYLIDENEACE&
Bis[(1E,4E)-1,5-bis(3,5-diMethoxyphenyl)…
diMethoxydibenzylideneacetone)palladiuM(0)
Bis(3,5,3',5'-dimethoxydibenzylideneacetone)
Bis(3,5,3',5'-dimethoxydibenzylideneacetone)palladium
Bis(3,3′,5,5′-dimethoxydibenzylideneacetone)palladium
PalladiuM,bis[(1E,4E)-(1,2,4,5-h)-1,5-bis(3,5-diMethoxyphenyl)
Bis(3,5,3',5'-diMethoxydibenzylideneacetone)palladiuM(0), Pd 13%
Bis(3,5,3’,5’-dimethoxydibenzylideneacetone)palladium(0) (Pd(dmdba)2)
PalladiuM,bis[(1E,4E)-(1,2,4,5-h)-1,5-bis(3,5-diMethoxyphenyl)-1,4-pentadien-3-one]-
[Molecular Formula]

2C21H22O5.Pd
[MDL Number]

MFCD07369799
[MOL File]

811862-77-8.mol
[Molecular Weight]

815.22
Chemical PropertiesBack Directory
[Melting point ]

170-178 °C(lit.)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

Powder
[color ]

Red-brown
[Water Solubility ]

Insoluble in water.
[InChI]

InChI=1S/2C21H22O5.Pd/c2*1-23-18-9-15(10-19(13-18)24-2)5-7-17(22)8-6-16-11-20(25-3)14-21(12-16)26-4;/h2*5-14H,1-4H3;/b2*7-5+,8-6+;
[InChIKey]

RTGAJOPJZJDWAX-XVGSOSPHSA-N
[SMILES]

[CH](C1=CC(OC)=CC(OC)=C1)[CH]C(=O)[CH][CH]C1=CC(OC)=CC(OC)=C1.[CH](C1=CC(OC)=CC(OC)=C1)[CH]C(=O)[CH][CH]C1=CC(OC)=CC(OC)=C1.[Pd] |^1:0,11,14,15,26,37,40,41|
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338-P280a-P304+P340-P405-P501a
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

suzuki reaction
[General Description]

Bis(3,5,3′,5′-dimethoxydibenzylideneacetone)palladium(0) is a non-phosphine based Pd(0) catalyst that can catalyze the Suzuki–Miyaura reaction of aryl chlorides with arylboronic acids with higher percentage conversion when compared to tris(dibenzylideneacetone)dipalladium(0) [Pd2(dba)3].
[reaction suitability]

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst
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