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Merck
CN

275891

Sigma-Aldrich

(1,5-环辛二烯)二氯化钯(II)

99%

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别名:
PdCl 2 (cod)
经验公式(希尔记法):
C8H12Cl2Pd
CAS号:
分子量:
285.51
EC 号:
MDL编号:
UNSPSC代码:
12352300
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

反应适用性

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Cross Couplings
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

mp

210 °C (dec.) (lit.)

SMILES字符串

Cl[Pd]Cl.C1CC=CCCC=C1

InChI

1S/C8H12.2ClH.Pd/c1-2-4-6-8-7-5-3-1;;;/h1-2,7-8H,3-6H2;2*1H;/q;;;+2/p-2/b2-1-,8-7-;;;

InChI key

RRHPTXZOMDSKRS-PHFPKPIQSA-L

应用

二氯(1,5-环辛二烯)钯 (II) 是常用的保护醇类缩醛的催化剂。以丙二酸二乙酯为原料,经烯烃羰基化合成双环辛烷。也可用于催化未活化的乙烯磷酸酯与缺电子烯烃的 Heck 偶联反应;从噻吩合成苯并[b]噻吩,并制备用于 Mizoroki-Heck 和 Suzuki-Miyaura 交叉偶联反应的活性催化剂。
用于 C-C 键和 C-N 形成的催化剂,用于炔烃与烯烃的 Heck 偶联,芳基溴化物的 Suzuki 交叉偶联,肟与烯丙基乙酸酯的烯丙基取代,和碘苯的甲氧基羰基化。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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An inexpensive and highly stable ligand 1, 4-bis (2-hydroxy-3, 5-di-tert-butylbenzyl) piperazine for Mizoroki?Heck and room temperature Suzuki?Miyaura cross-coupling reactions.
Mohanty S, et al.
Tetrahedron, 64(1), 240-247 (2008)
Palladium-catalysed direct synthesis of benzo [b] thiophenes from thioenols.
Inamoto K, et al.
Chemical Communications (Cambridge, England), 43, 5529-5531 (2008)
Studies on the Heck reaction with alkenyl phosphates: Can the 1, 2-migration be controlled? Scope and Limitations.
Ebran J P, et al.
Journal of the American Chemical Society, 129(21), 6931-6942 (2007)
Dichloro(1,5?cyclooctadiene)palladium(II).
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2009)
Eda Rami Reddy et al.
Dalton transactions (Cambridge, England : 2003), 44(40), 17600-17616 (2015-09-24)
A series of five palladium(ii) pyridyl-imine Schiff base complexes 5a-e containing boronate esters with protected sugar diols derived from d-xylose, l-sorbose and d-mannitol were designed and synthesized starting from pyridyl-imines generated in situ from 3-aminophenyl boronate ester of sugars 3a-e

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