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文件

764299

APhos Pd G2

Name: APhos Pd G2
Brand: ALDRICH

别名:

APhos-Pd-G2, Chloro[4-(di-tert-butylphosphino)-N,N-dimethylaniline-2-(2′-aminobiphenyl)]palladium(II)

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About This Item

经验公式（希尔记法）:

C₂₈H₃₈ClN₂PPd

CAS号:

2169976-34-3

分子量:

575.46

MDL號碼:

MFCD22417237

分類程式碼代碼:

12161600

PubChem物質ID:

329767111

NACRES:

NA.22

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双(三叔丁基膦)钯(0)

形狀

solid

特點

generation 2

反應適用性

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

雜質

<2% Acetone

官能基

phosphine

SMILES 字串

Nc1ccccc1-c2ccccc2[Pd]Cl.CN(C)c3ccc(cc3)P(C(C)(C)C)C(C)(C)C

InChI

1S/C16H28NP.C12H10N.ClH.Pd/c1-15(2,3)18(16(4,5)6)14-11-9-13(10-12-14)17(7)8;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h9-12H,1-8H3;1-6,8-9H,13H2;1H;/q;;;+1/p-1

InChI 密鑰

LRWGTPCCIGPYMI-UHFFFAOYSA-M

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儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

分析证书(COA)

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商品

2nd Generation Buchwald Precatalysts

Buchwald precatalysts and ligands are bulky electron-rich dialkylbiaryl phospine-based catalysts and structurally related ligands that improve reactivity in Pd-catalyzed cross - coupling reactions

The Buchwald group has developed a series of highly active and versatile palladium precatalysts and biarylphosphine ligands used in cross-coupling reactions for the formation of C-C, C–N, C–O, C–F, C–CF3, and C–S bonds. The ligands are electron-rich, and highly tunable to provide catalyst systems with a diverse scope, high stability and reactivity. Furthermore, the new series of precatalysts are air-, moisture and thermally-stable and display good solubility in common organic solvents. The use of precatalysts ensures the efficient generation of the active catalytic species and allows one to accurately adjust the ligand:palladium ratio. The ligands, precatalysts and methodology developed in the Buchwald group are user friendly and have rendered previously difficult cross couplings reactions, much easier to achieve.

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