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Merck

647640

Sigma-Aldrich

氯化锆(IV)

anhydrous, powder, 99.99% trace metals basis

别名:

四氯化锆, 氯化锆

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About This Item

线性分子式:
ZrCl4
CAS号:
分子量:
233.04
EC號碼:
MDL號碼:
分類程式碼代碼:
12352302
PubChem物質ID:
NACRES:
NA.23
化驗:
99.99% trace metals basis
等級:
anhydrous
形狀:
powder

等級

anhydrous

品質等級

蒸汽壓力

1 mmHg ( 190 °C)

化驗

99.99% trace metals basis

形狀

powder

反應適用性

reagent type: catalyst
core: zirconium

雜質

<50 ppm hafnium

轉變溫度

sublimation point 331 °C

密度

2.8 g/mL at 25 °C (lit.)

應用

battery manufacturing

SMILES 字串

Cl[Zr](Cl)(Cl)Cl

InChI

1S/4ClH.Zr/h4*1H;/q;;;;+4/p-4

InChI 密鑰

DUNKXUFBGCUVQW-UHFFFAOYSA-J

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一般說明

氯化锆(IV) (ZrCl4)是一种路易斯酸催化剂,毒性低。它是一种防潮材料,在有机转化中用作催化剂。

應用

ZrCl4 可作为各种有机合成的催化剂,如Friedel-Crafts反应、缩合反应和其他还原反应。

象形圖

Corrosion

訊號詞

Danger

危險聲明

危險分類

Met. Corr. 1 - Skin Corr. 1B

安全危害

儲存類別代碼

8B - Non-combustible corrosive hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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分析证书(COA)

Lot/Batch Number

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其他客户在看

Erik A Wu et al.
Nature communications, 12(1), 1256-1256 (2021-02-25)
Rechargeable solid-state sodium-ion batteries (SSSBs) hold great promise for safer and more energy-dense energy storage. However, the poor electrochemical stability between current sulfide-based solid electrolytes and high-voltage oxide cathodes has limited their long-term cycling performance and practicality. Here, we report
Applications of zirconium (IV) chloride in organic synthesis
Smitha G, et al.
Synthesis, 2008(06), 829-855 (2008)
Stefania Fioravanti et al.
Organic & biomolecular chemistry, 10(41), 8207-8210 (2012-09-26)
ZrCl(4) was found to be an ideal catalyst to promote aza-Henry reactions between trifluoromethyl aldimines and some nitro alkanes giving new fluorinated β-nitro amines. The reaction is strongly influenced by the CF(3) group, the yield by the alkyl chain of
Abed Al Aziz Quntar et al.
The Journal of organic chemistry, 71(2), 730-733 (2006-01-18)
[reaction: see text] The reagent system Cp2ZrCl2/2EtMgBr/2AlCl3 converts 1-alkynylphosphonates into cyclopropylmethylphosphonates 3 in good isolated yields. Ethers, chlorides, and other cyclopropyl groups are compatible with the reaction conditions. Deuterium labeling is consistent with the formation of stable cyclopropylmethylbimetallic phosphonates by
Direct amide coupling of non-activated carboxylic acids and amines catalysed by zirconium(IV) chloride.
Helena Lundberg et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(13), 3822-3826 (2012-03-01)

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