ChemicalBook--->CAS DataBase List--->1447963-75-8

1447963-75-8

1447963-75-8 Structure

1447963-75-8 Structure
IdentificationBack Directory
[Name]

tBuXPhos Pd G3
[CAS]

1447963-75-8
[Synonyms]

tBuXPhos Pd G3
tBuXPhos Pd G3 97%
Methanesulfonato(2-di-t-butylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II)
[(2-Di-tert-butylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)-2-(2′-amino-1,1′-biphenyl)] palladium(II) methanesulfonate
Methanesulfonato(2-di-t-butylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II), min. 98%
[2'-(Amino)[1,1'-biphenyl]-2-yl][bis(1,1-dimethylethyl)[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine](methanesulfonato)palladium
Methanesulfonato(2-di-t-butylphosphino-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-aMino-1,1'-biphenyl-2-yl)palladiuM(II), Min. 98% [t-BuXPhos Palladacycle]
Palladium, [2'-(amino-κN)[1,1'-biphenyl]-2-yl-κC][bis(1,1-dimethylethyl)[2',4',6'-tris(1-methylethyl)[1,1'-biphenyl]-2-yl]phosphine](methanesulfonato-κO)-
[Molecular Formula]

C42H58NO3PPdS
[MDL Number]

MFCD22666411
[MOL File]

1447963-75-8.mol
[Molecular Weight]

794.38
Chemical PropertiesBack Directory
[Melting point ]

130-140°C
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[form ]

Powder
[color ]

yellow
[InChIKey]

KKVLHKIBKWORMK-UHFFFAOYSA-N
[SMILES]

P(C1C=CC=CC=1C1C(=CC(C(C)C)=CC=1C(C)C)C(C)C)([Pd+2]1(NC2=CC=CC=C2C2=CC=CC=[C-]12)[O-]S(=O)(=O)C)(C(C)(C)C)C(C)(C)C
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[WGK Germany ]

3
[HS Code ]

2843909000
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Physical properties]

tBuXPhos-Pd-G3 is in the form of a dark grey crystalline powder.
[Uses]

tBuXPhos Pd G3 may be used to synthesize 4-cyano-7-azaindole from 4-chloro-7-azaindole by cyanation reaction. It may also be used for the α-arylation reaction of acetate esters at room temperature.
[Reactions]

Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media.
Reactions of 1447963-75-8
[General Description]

tBuXPhos Pd G3(1447963-75-8) is a third generation (G3) Buchwald precatalyst. It is air, moisture and thermally-stable and is highly soluble in a wide range of common organic solvents. It has long life in solutions. tBuXPhos Pd G3 is an excellent reagent for Buchwald-Hartwig cross-coupling reaction. Some of its unique features include lower catalyst loadings, shorter reaction time, efficient formation of the active catalytic species and accurate control of ligand: palladium ratio.
[reaction suitability]

reagent type: catalyst
reaction type: Cross Couplings
[storage]

tBuXPhos Pd G3 should be stored in an airtight, dry and low temperature.
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