937401
(tBuXPhos)Pd(p-TMSCH2CH2CO2C6H4)(Br)
≥95%, powder or crystals
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About This Item
Empirical Formula (Hill Notation):
C41H62BrO2PPdSi
CAS Number:
Molecular Weight:
832.31
UNSPSC Code:
12352142
NACRES:
NA.21
Product Name
(tBuXPhos)Pd(p-TMSCH2CH2CO2C6H4)(Br), ≥95%
Quality Level
Assay
≥95%
form
powder or crystals
reaction suitability
reaction type: Cross Couplings
greener alternative product characteristics
Catalysis
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color
white to faint yellow
functional group
(Palladium)
phosphine
greener alternative category
storage temp.
room temp
SMILES string
Br[Pd](C1=CC=C(C(OCC[Si](C)(C)C)=O)C=C1)[P](C2=CC=CC=C2C3=C(C(C)C)C=C(C(C)C)C=C3C(C)C)(C(C)(C)C)C(C)(C)C
Related Categories
General description
(tBuXPhos)Pd(p-TMSCH2CH2CO2C6H4)(Br) is a G6 Buchwald precatalyst. The G6 precatalysts are air-stable, palladium-based oxidative addition complexes (OACs) that offer an alternative to the previously developed classes of palladacycle precatalysts. Unlike previous generations, the bulkiest biarylphosphine ligand precatalysts are readily prepared. These precatalysts have been shown to be effective for many reactions, including C-N, C-O, and C-F cross couplings.
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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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Ryan P King et al.
Organic letters, 23(20), 7927-7932 (2021-10-07)
The utilization of isolated Palladium Oxidative Addition Complexes (OACs) has had a significant impact on Pd-catalyzed and Pd-mediated cross-coupling reactions. Despite their importance, widespread utility of OACs has been limited by the instability of their precursor complexes. Herein, we report
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