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Merck
CN

900472

Sigma-Aldrich

(R)-TolBINAP Pd G4

95%, powder

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About This Item

Empirical Formula (Hill Notation):
C62H55NO3P2PdS
Molecular Weight:
1062.54
UNSPSC Code:
12161600
NACRES:
NA.22

Key Documents

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Product Name

(R)-TolBINAP Pd G4, 95%

Quality Level

100

Assay

95%

form

powder

feature

generation 4

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
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
reaction type: Cross Couplings

functional group

phosphine

SMILES string

CC(C=C1)=CC=C1P(C2=CC=C(C)C=C2)C3=C(C4=C(P(C5=CC=C(C)C=C5)C6=CC=C(C)C=C6)C=CC7=C4C=CC=C7)C8=C(C=C3)C=CC=C8.C[NH+](C9=C(C=CC=C9)C%10=C%11C=CC=C%10)[Pd-]%11OS(C)(=O)=O

InChI key

WKGRPDDVBKRQJX-UHFFFAOYSA-M

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCB9571

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Nathaniel H Park et al.
Angewandte Chemie (International ed. in English), 54(28), 8259-8262 (2015-06-03)
In Pd-catalyzed C-N cross-coupling reactions, α-branched secondary amines are difficult coupling partners and the desired products are often produced in low yields. In order to provide a robust method for accessing N-aryl α-branched tertiary amines, new catalysts have been designed

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