221880
氯化锆(IV)
≥99.5% trace metals basis
别名:
四氯化锆, 氯化锆
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关于此项目
线性分子式:
ZrCl4
化学文摘社编号:
分子量:
233.04
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
233-058-2
MDL number:
Assay:
≥99.5% trace metals basis
Form:
powder
InChI key
DUNKXUFBGCUVQW-UHFFFAOYSA-J
InChI
1S/4ClH.Zr/h4*1H;/q;;;;+4/p-4
SMILES string
Cl[Zr](Cl)(Cl)Cl
vapor pressure
1 mmHg ( 190 °C)
assay
≥99.5% trace metals basis
form
powder
reaction suitability
core: zirconium, reagent type: catalyst
greener alternative product characteristics
Catalysis
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sustainability
Greener Alternative Product
impurities
≤5000.0 ppm Trace Metal Analysis
transition temp
sublimation point 331 °C
density
2.8 g/mL at 25 °C (lit.)
greener alternative category
, Aligned
Quality Level
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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。点击此处以获取更多信息。
Application
signalword
Danger
hcodes
Hazard Classifications
Met. Corr. 1 - Skin Corr. 1B
supp_hazards
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
Ines Sifaoui et al.
Frontiers in bioengineering and biotechnology, 9, 584115-584115 (2021-02-19)
In this study, the application of amphipods in vivo assays was evaluated. The main aim of this work was to check the potential use of this model in biocompatibility assessments of metal-organic frameworks (MOFs). Hence, six different MOFs were synthesized
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
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
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.
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.
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