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Merck
CN

196215

双(环戊二烯基)二氯化锆(IV)

greener alternative

≥98%, solid

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

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关于此项目

经验公式(希尔记法):
C10H10Cl2Zr
化学文摘社编号:
分子量:
292.32
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12161600
EC Number:
215-066-8
MDL number:
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产品名称

双(环戊二烯基)二氯化锆(IV), ≥98%

InChI key

QRUYYSPCOGSZGQ-UHFFFAOYSA-L

InChI

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

SMILES string

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

assay

≥98%

form

solid

reaction suitability

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

greener alternative product characteristics

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

parameter

moisture sensitive

mp

242-245 °C (lit.)

greener alternative category

storage temp.

2-8°C

Quality Level

General description

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。

Application

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。

signalword

Warning

pictograms

Exclamation mark

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Wen-Xiong Zhang et al.
Accounts of chemical research, 44(7), 541-551 (2011-05-27)
Characterizing reactive organometallic intermediates is critical for understanding the mechanistic aspects of metal-mediated organic reactions. Moreover, the isolation of reactive organometallic intermediates can often result in the ability to design new synthetic methods. In this Account, we outline synthetic methods
Christine Bibal et al.
Dalton transactions (Cambridge, England : 2003), (21)(21), 2866-2870 (2008-05-15)
A new family of hydroxytris(pentafluorophenyl)borate anions [B(C6F5)3OH](-) associated with organic and aprotic cations c+ (imidazolium, pyrrolidinium and phosphonium) has been prepared by a general one-pot synthesis that implies the chloride borate analogues [B(C6F5)3Cl](-)[c]+. The [c]+[B(C6F5)3OH](-) salts have been isolated and
Andy M Chapman et al.
Journal of the American Chemical Society, 133(45), 18463-18478 (2011-10-01)
The extension of the frustrated Lewis pair (FLP) concept to the transition series with cationic zirconocene-phosphinoaryloxide complexes is demonstrated. Such complexes mimic the reactivity of main group FLPs in reactions such as heterolytic hydrogen cleavage, CO(2) activation, olefin and alkyne
José Barluenga et al.
Organic letters, 9(16), 3081-3084 (2007-07-20)
A new regio- and stereoselective zirconocene-catalyzed reaction for the synthesis of medium-sized rings is described. The global reaction supposes a formal ring expansion of a cyclic enol ether to give a functionalized carbocycle.
Sven Tobisch
Dalton transactions (Cambridge, England : 2003), (35)(35), 4277-4285 (2006-08-26)
The complete sequence of steps of a tentative catalytic cycle for intramolecular hydroamination/cyclisation (IHC) of 4,5-hexadien-1-ylamine (1) by a prototypical cationic [Cp(2)ZrCH(3)](+) zirconocene precatalyst (2) has been examined by employing a gradient-corrected DFT method. The predicted smooth overall reaction energy

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