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Merck
CN

768154

2-(二-1-金刚烷基膦基)-3,6-二甲氧基-2′,4′,6′-三异丙基-1,1′ - 联苯

95%, solid

别名:

2-(二-1-金刚烷基膦)-3,6-二甲氧基-2′,4′,6′-三异丙基-1,1′-联苯

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关于此项目

经验公式(希尔记法):
C43H61O2P
化学文摘社编号:
分子量:
640.92
MDL number:
UNSPSC Code:
12352112
PubChem Substance ID:
NACRES:
NA.22
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产品名称

2-(二-1-金刚烷基膦基)-3,6-二甲氧基-2′,4′,6′-三异丙基-1,1′ - 联苯, 95%

Quality Level

product line

Buchwald Ligand

assay

95%

form

solid

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: ligand

mp

231-235 °C

functional group

phosphine

SMILES string

COc1ccc(OC)c(c1P(C23CC4CC(CC(C4)C2)C3)C56CC7CC(CC(C7)C5)C6)-c8c(cc(cc8C(C)C)C(C)C)C(C)C

InChI

1S/C43H61O2P/c1-25(2)34-17-35(26(3)4)39(36(18-34)27(5)6)40-37(44-7)9-10-38(45-8)41(40)46(42-19-28-11-29(20-42)13-30(12-28)21-42)43-22-31-14-32(23-43)16-33(15-31)24-43/h9-10,17-18,25-33H,11-16,19-24H2,1-8H3

InChI key

NMGHOZQCYNKWBG-UHFFFAOYSA-N

General description

AdBrettPhos 是一种膦基配体,用于氨的直接单芳基化,并抑制二芳基化。此外,它也是五元杂芳烃偶联的良好配体,并用于制备膦连接的钯复合物,以促进C-N偶联反应。

Application

AdBrettPhos 可用作合成[(L·Pd)n ·(1,5-环辛二烯)]预催化剂的有效配体,该预催化剂可用于芳基三氟甲磺酸酯的钯催化氟化。

AdBrettPhos可用于钯催化的一级醇的C-O交叉偶联。


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)

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商品

Discover AdQPhos and its Pd pre-catalysts for selective α-arylation of diverse nucleophiles under mild aqueous conditions without hazardous solvents.

相关内容

Explore reliable, premium grade catalysis materials for your pharma or industrial project. Specialty chemicals and formulations are available in bulk quantities and volumes from a few grams to multi-metric tons with complete documentation to simplify your leap from development to commercialization.

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.


A Bulky Biaryl Phosphine Ligand Allows for Palladium-Catalyzed Amidation
Angewandte Chemie (International Edition in English), 51, 1-5 (2012)
Structure and reactivity of [(L?Pd)n?(1,5-cyclooctadiene)] (n = 1?2) complexes bearing biaryl phosphine ligands
Lee HG, et al.
Inorganica chimica acta, 422, 188-192 (2014)



全球贸易项目编号

货号GTIN
768154-500MG04061833441107
768154-100MG04061833441091
768154-1G04061826654651