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等級
anhydrous
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。
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
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
Synthesis of 2, 3-dihydroquinazolin-4 (1H)-ones catalyzed by zirconium (IV) chloride as a mild and efficient catalyst
Abdollahi-Alibeik M and Shabani E
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 22(10), 1163-1166 (2011)
Awakening a dormant catalyst: salicylaldimine systems for ethene/tert-butylstyrene copolymerization.
Giles W Theaker et al.
Dalton transactions (Cambridge, England : 2003), (48)(48), 6883-6885 (2008-12-04)
A group of readily available zirconium catalysts incapable of ethene-co-styrene polymerization are remarkably active and selective for the production of the new polymer ethene-co-tert-butylstyrene via a single site mechanism.
Harish Kumar et al.
Ultrasonics sonochemistry, 15(2), 129-132 (2007-04-17)
Sonication of aromatic aldehydes, urea and ethyl acetoacetate in presence of solvent (ethyl alcohol) or solvent-less dry media (bentonite clay) supported-zirconium (IV) chloride (ZrCl(4)) as catalyst at 35 kHz gives 6-methyl-4-substitutedphenyl-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylic acid ethyl esters proficiently in high yields.
Thomas A Dineen et al.
Journal of the American Chemical Society, 128(50), 16406-16409 (2006-12-15)
Two protocols for the transamidation of primary amides with primary and secondary amines, forming secondary and tertiary amides, respectively, are described. Both processes employ N,N-dialkylformamide dimethyl acetals for primary amide activation, producing N'-acyl-N,N-dialkylformamidines as intermediates, as widely documented in the
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