跳转至内容
Merck
CN

196215

Sigma-Aldrich

双(环戊二烯基)二氯化锆(IV)

greener alternative

≥98%

别名:

二氯二茂, 二氯化双环戊二烯锆, 二氯双环戊二烯锆, 二(环戊二烯基)二氯化锆(IV), 二氯二茂锆

登录查看公司和协议定价


About This Item

经验公式(希尔记法):
C10H10Cl2Zr
CAS号:
分子量:
292.32
EC 号:
MDL编号:
UNSPSC代码:
12161600
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥98%

表单

solid

反应适用性

core: zirconium
reaction type: Polymerization Reactions
reagent type: catalyst
reaction type: Olefin Metathesis

环保替代产品特性

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

参数

moisture sensitive

mp

242-245 °C (lit.)

环保替代产品分类

储存温度

2-8°C

SMILES字符串

Cl[Zr]Cl.[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2

InChI

1S/2C5H5.2ClH.Zr/c2*1-2-4-5-3-1;;;/h2*1-5H;2*1H;/q;;;;+2/p-2

InChI key

QRUYYSPCOGSZGQ-UHFFFAOYSA-L

正在寻找类似产品? 访问 产品对比指南

一般描述

我们致力于为您提供更环保的替代产品,以符合“绿色化学的12项原则”的一项或多项原则要求。该产品为增强型,提高了催化效率。详细信息见于此处

二氯二茂锆可用作催化剂,从而实现吡咯的高效催化,产率高,简化纯化过程。

应用

用于促进催化量的羧酸和胺的绿色酰胺化。该技术避免了羧酸预活化或使用偶联试剂的要求。

未活化羧酸和胺直接生成酰胺
用于合成多种前过渡金属和有机金属化合物。

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

储存分类代码

11 - Combustible Solids

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


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

Yuushou Nakayama et al.
Molecules (Basel, Switzerland), 10(6), 620-633 (2007-11-17)
This review article describes developments in chiral metallocenes as polymerization catalysts focusing on C2 symmetric ansa-zirconocene complexes. Selective synthesis of rac-isomers of ansa-zirconocenes are surveyed. Isospecific polymerizations of propylene catalyzed by chiral zirconocenes are summarized. Advanced series of polymerizations by
Vidar R Jensen et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 6(9), 1929-1933 (2005-08-03)
Free Car-Parrinello molecular dynamics (CPMD) simulations of four diastereomers of the zirconium-propene complexes [{iPr(3-iPr-CpFlu)}ZriBu(C3H6)]+ (Cp=cyclopentadienyl; Flu=fluorenyl) provide valuable insight into the mechanism and stereocontrol of propene polymerization with stereorigid metallocenes. Spontaneous insertion of propene into the zirconium-isobutyl bond is not
Leo A Paquette et al.
Organic letters, 7(3), 511-513 (2005-01-28)
[reaction: see text] A synthetic route to select cyclooctane-1,2,3-triols and 1,2,3,4,5-pentaols has been defined. The starting materials are d-glucose or d-arabinose, and the key steps consist of a zirconocene-promoted ring contraction, a [3,3] sigmatropic rearrangement, and more extended functionalization of
Zirconocene dichloride catalysed one-pot synthesis of pyrroles through nitroalkene-enamine assembly
Goyal S, et al.
Royal Society of Chemistry Advances, 5, 3187-3195 (2015)
Anita Lagutschenkov et al.
The journal of physical chemistry. A, 114(5), 2073-2079 (2010-01-21)
Cationic zirconocene complexes are active species in Ziegler-Natta catalysis for olefin polymerization. Their structure and metal-ligand bond strength strongly influence their activity. In the present work, the infrared multiphoton dissociation (IRMPD) spectrum of mass selected Zr(C(5)H(5))(2)(OH)(CH(3)CN)(+) cations was obtained in

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.

联系技术服务部门