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Merck
CN

937401

(tBuXPhos)Pd(p-TMSCH2CH2CO2C6H4)(Br)

greener alternative

≥95%, powder or crystals

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关于此项目

经验公式(希尔记法):
C41H62BrO2PPdSi
化学文摘社编号:
分子量:
832.31
UNSPSC Code:
12352142
NACRES:
NA.21
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产品名称

(tBuXPhos)Pd(p-TMSCH2CH2CO2C6H4)(Br), ≥95%

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

assay

≥95%

form

powder or crystals

reaction suitability

reaction type: Cross Couplings

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

color

white to faint yellow

functional group

(Palladium)
phosphine

greener alternative category

storage temp.

room temp

Quality Level

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.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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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