主要文件

查看所有文档

900534

（t-Bu）PhCPhos Pd G3

Name: （t-Bu）PhCPhos Pd G3
Brand: ALDRICH

≥95%, powder

登录查看组织和合同定价。

选择尺寸

变更视图

关于此项目

经验公式（希尔记法）:

C₃₉H₄₆N₃O₃PPdS

化学文摘社编号:

1661042-31-4

分子量:

774.26

MDL number:

MFCD31560638

UNSPSC Code:

12161600

NACRES:

NA.22

技术服务

需要帮助？我们经验丰富的科学家团队随时乐意为您服务。

让我们为您提供帮助

属性

产品名称

（t-Bu）PhCPhos Pd G3, ≥95%

Quality Level

100

product line

Buchwald precatalyst Generation 3

assay

≥95%

form

powder

feature

generation 3

reaction suitability

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

[Pd+2]c4c(cccc4)c5c(cccc5)[N-H].P(C(C)(C)C)(c2c(cccc2)c3c(cccc3N(C)C)N(C)C)c1ccccc1.[S](=O)(=O)([O-])C

InChI

1S/C26H33N2P.C12H9N.CH4O3S.Pd/c1-26(2,3)29(20-14-9-8-10-15-20)24-19-12-11-16-21(24)25-22(27(4)5)17-13-18-23(25)28(6)7;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h8-19H,1-7H3;1-6,8-9,13H;1H3,(H,2,3,4);/q;-1;;+2/p-1

InChI key

IYOQFXCZIJAOED-UHFFFAOYSA-M

说明

Application

作为Pd G3络合物，来自Buchwald小组的这种配体催化剂在空间受阻的伯胺的芳基化反应中提供了同类产品中最佳的反应活性。

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our 文件 section.

如需帮助，请联系客户支持

已有该产品？

在文件库中查找您最近购买产品的文档。

访问文档库

商品

G3和G4 Buchwald预催化剂

G3和G4 Buchwald预催化剂是一类最新的空气、湿度和热稳定型交叉偶联复合物，可用于键形成以实现其多功能性和高反应性。

G3 and G4 Buchwald Precatalysts

G3 and G4 Buchwald palladium precatalysts are the newest air, moisture, and thermally stable crossing-coupling complexes used in bond formation for their versatility and high reactivity.

Rational ligand design for the arylation of hindered primary amines guided by reaction progress kinetic analysis.

Paula Ruiz-Castillo et al.

Journal of the American Chemical Society, 137(8), 3085-3092 (2015-02-05)

We report the Pd-catalyzed arylation of very hindered α,α,α-trisubstituted primary amines. Kinetics-based mechanistic analysis and rational design have led to the development of two biarylphosphine ligands that allow the transformation to proceed with excellent efficiency. The process was effective in

全球贸易项目编号

货号	GTIN
900534-250MG	04061833250266