跳转至内容
Merck
CN

481408

二环己基氯化膦

97%

别名:

二环己基次膦酰氯, 二环己基氯化膦, 二环己基氯膦

登录 查看组织和合同定价。

选择尺寸


关于此项目

线性分子式:
(C6H11)2PCl
化学文摘社编号:
分子量:
232.73
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
MDL number:
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
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

产品名称

二环己基氯化膦, 97%

InChI

1S/C12H22ClP/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-12H,1-10H2

SMILES string

ClP(C1CCCCC1)C2CCCCC2

InChI key

AKJFBIZAEPTXIL-UHFFFAOYSA-N

assay

97%

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

refractive index

n20/D 1.533 (lit.)

bp

165 °C/12 mmHg (lit.)

density

1.054 g/mL at 25 °C (lit.)

functional group

phosphine

Quality Level

Application

二环己基氯化膦可用作反应物参与合成:
  • 1,2-双(二环己基次膦氧基)乙烷配体(在存在三乙胺的情况下与乙二醇通过Michaelis−-Arbuzov重排反应)。
  • 1,1,2,2-四环己基二膦一硫化物配体(通过LiS处理)。

它还可用作原料制备其他配体,如二环己基氧化膦、膦基取代的N-芳基吡咯 、二丁基((二环己基膦基)甲基)膦 、二环己基环戊基膦。这些配体可用于钯催化的交叉偶联反应。

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

supp_hazards

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

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

Practical synthesis of new and highly efficient ligands for the Suzuki reaction of aryl chlorides
Zapf A, et al.
Chemical Communications (Cambridge, England), 19(1), 38-39 (2004)
A sulfur mimic of 1, 1-bis (diphenylphosphino) methane: a new ligand opens up
Sues PE, et al.
Chemical Communications (Cambridge, England), 50(36), 4707-4710 (2014)
Characterization of secondary phosphine oxide ligands on the surface of iridium nanoparticles
Cano I, et al.
Physical Chemistry Chemical Physics, 19(32), 21655-21662 (2017)
Simon Doherty et al.
Nature protocols, 7(10), 1870-1883 (2012-09-29)
This protocol describes the synthesis of a representative example of the electron-rich biaryl-like KITPHOS class of monophosphine, 11-dicyclohexylphosphino-12-phenyl-9,10-dihydro-9,10-ethenoanthracene (H-KITPHOS). The bicyclic architecture of H-KITPHOS is constructed via [4+2] Diels-Alder cycloaddition between 1-(dicyclohexylphosphinoylethynyl)benzene and anthracene. H-KITPHOS monophosphine is prepared via an
Synthesis of 1, 2-bis [(diorgano) phosphino] ethanes via Michaelis-Arbuzov type rearrangements
Baldwin LC and Fink MJ
Journal of Organometallic Chemistry, 646(1-2), 230-238 (2002)

相关内容

Phosphine Ligand Application Guide

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持