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Merck
CN

761435

[(二(1-金刚烷基)丁基膦基)-2-(2′-氨基-1,1′-联苯基)]钯(II)甲磺酸酯

greener alternative

95%, solid

别名:

[(二(1-金刚烷基)丁基膦基)-2-(2′-氨基-1,1′-联苯基)]钯(II) 甲磺酸酯, cataCXium-A-Pd-G3, 甲磺酸[(二(1-金刚烷基)丁基膦基)-2-(2′-氨基-1,1′-联苯基)]钯(II)

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关于此项目

经验公式(希尔记法):
C37H52NO3PPdS
化学文摘社编号:
分子量:
728.27
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.22
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产品名称

[(二(1-金刚烷基)丁基膦基)-2-(2′-氨基-1,1′-联苯基)]钯(II)甲磺酸酯, 95%

SMILES string

CS(=O)(=O)O[Pd]c1ccccc1-c2ccccc2N.CCCCP([C@@]34C[C@@H]5C[C@@H](C[C@@H](C5)C3)C4)[C@@]67C[C@@H]8C[C@@H](C[C@@H](C8)C6)C7

InChI

1S/C24H39P.C12H10N.CH4O3S.Pd/c1-2-3-4-25(23-11-17-5-18(12-23)7-19(6-17)13-23)24-14-20-8-21(15-24)10-22(9-20)16-24;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;1-5(2,3)4;/h17-22H,2-16H2,1H3;1-6,8-9H,13H2;1H3,(H,2,3,4);/q;;;+1/p-1/t17-,18+,19-,20-,21+,22-,23-,24-;;;

InChI key

REYVZCOGMIXVNX-DVBMAMJVSA-M

assay

95%

form

solid

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

greener alternative product score

old score: 16
new score: 2
Find out more about DOZN™ Scoring

greener alternative product characteristics

Waste Prevention
Atom Economy
Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

impurities

≤3% acetone

mp

196-241 °C (decomposition)

functional group

phosphine

greener alternative category

Quality Level

Application

cataCXium® A Pd G3 是一种第三代Buchwald预催化剂,可用于:
  • 吡啶羧酸的直接邻位芳基化。
  • 催化Suzuki–Miyaura交叉偶联反应,以合成1-杂芳基-3-氮杂双环[3.1.0]己烷。
  • 炔烃的钯催化羰基碳全氟烷基化。
  • 各种 gem二取代环丙烷的合成过程中成对二(溴基)环丙烷的Suzuki–Miyaura 偶联反应。
  • 末端炔烃的溴全氟烷基化。
  • 芳香卤化物和炔烃的无铜Sonogashira 偶联反应,以形成 C-C键。
  • 有机三氟硼酸盐和芳基卤化物的Suzuki 交叉偶联反应。
对于小规模和高通量用途,产品为ChemBeads ChemBeads (928305)

General description

我们竭诚为您带来满足绿色替代产品四大类别要求的替代产品。 本产品属于重新设计产品类别,在绿色化学原理“防止废弃物”、“更安全的溶剂和助剂”以及“原子经济”方面有重大改进。点击此处查看其 DOZN 记分卡。

Legal Information

cataCXium is a registered trademark of Umicore AG & Co. KG

存储类别

13 - Non 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

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Construction of 1-Heteroaryl-3-azabicyclo [3.1. 0] hexanes by sp3-sp2 Suzuki-Miyaura and Chan-Evans-Lam Coupling Reactions of Tertiary Trifluoroborates.
Harris MR, et al.
Organic Letters, 19(9), 2450-2453 (2017)
Copper-free Sonogashira cross-coupling reactions: an overview
Mohajer F, et al.
Royal Society of Chemistry Advances, 11, 6885-6925 (2021)
Rapid access to diverse, trifluoromethyl-substituted alkenes using complementary strategies
Phelan J, et al.
Chemical Science, 9, 3215-3220 (2018)
Direct ortho-Arylation of Pyridinecarboxylic Acids: Overcoming the Deactivating Effect of sp2-Nitrogen.
Johnston AJS, et al.
Organic Letters, 18(23), 6094-6097 (2016)
The use of carboxylic acids as traceless directing groups for regioselective C-H bond functionalisation.
Font M and Quibell
Chemical Communications (Cambridge, England), 53(41), 5584-5597 (2017)

商品

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.

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

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

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

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