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About This Item
線性公式:
ZrCl4
CAS號碼:
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
推薦產品
等級
for analytical purposes
蒸汽壓力
1 mmHg ( 190 °C)
化驗
≥99.5% trace metals basis
形狀
powder
反應適用性
reagent type: catalyst
core: zirconium
環保替代產品特色
Catalysis
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sustainability
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雜質
≤5000.0 ppm Trace Metal Analysis
轉變溫度
sublimation point 331 °C
密度
2.8 g/mL at 25 °C (lit.)
應用
battery manufacturing
環保替代類別
, Aligned
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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應用
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
8A - 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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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
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We have surveyed the utility of Beckmann rearrangement for the conversion of indanones into carbostyrils. Initial attempts at the conversion of 6-methoxy indanone oxime under classical conditions resulted in the formation of the two unusual products: 2-sulfonyloxyindanone and the dimeric
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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