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Merck

764183

Sigma-Aldrich

APhos Pd G3

greener alternative

97%

別名:

APhos-Pd-G3, [4-(ジ-tert-ブチルホスフィノ)-N,N-ジメチルアニリン-2-(2′-アミノビフェニル)]パラジウム(II)メタンスルホン酸, パラジウムG3-(4-(N,N-ジメチルアミノ)フェニル)ジ-tert-ブチルホスフィン

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About This Item

実験式(ヒル表記法):
C29H41N2O3PPdS
CAS番号:
分子量:
635.11
MDL番号:
UNSPSCコード:
12161600
PubChem Substance ID:
NACRES:
NA.22

品質水準

アッセイ

97%

形状

solid

特徴

generation 3

反応適合性

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

環境により配慮した代替製品スコア

old score: 5
new score: 3
Find out more about DOZN™ Scoring

環境により配慮した代替製品の特徴

Waste Prevention
Atom Economy
Less Hazardous Chemical Syntheses
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

192-201 °C (decomposition)

官能基

phosphine

環境により配慮した代替製品カテゴリ

SMILES記法

NC1=C(C=CC=C1)C2=C([Pd]OS(C)(=O)=O)C=CC=C2.CN(C)C3=CC=C(C=C3)P(C(C)(C)C)C(C)(C)C

InChI

1S/C16H28NP.C12H10N.CH4O3S.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;1-5(2,3)4;/h9-12H,1-8H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1

InChI Key

SNUBBUQVCDWEAV-UHFFFAOYSA-M

詳細

We are committed to bringing you Greener Alternative Products, which adhere to one of the four categories of Greener Alternatives. This product belongs to category of Re-engineered products, showing key improvements in Green Chemistry Principles “Waste Prevention”, “Atom Economy” and “Less Hazardous Chemical Synthesis”. Click here to view its DOZN scorecard.

アプリケーション

APhos Pd G3は、クロスカップリング反応に使用できるBuchwaldプレ触媒です。

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable


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Synthesis of Double-Bond-Substituted Hemithioindigo Photoswitches
Gerwien A, et al.
Organic Letters, 20(1), 232-235 (2018)
Capture of reactive monophosphine-ligated palladium (0) intermediates by mass spectrometry
Zheng Q, et al.
Journal of the American Chemical Society, 137(44), 14035-14038 (2015)

資料

All of the preformed catalysts used in the kit are air and moisture stable complexes in their commercially available form.

Tools aid in kit setup for organic chemistry techniques, ensuring ease and success.

Materials Included in your KITALYSIS-24PD-2PK High-Throughput Screening Kit

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.

関連コンテンツ

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.

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.

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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