249955
氯化锡(IV) 溶液
1.0 M in methylene chloride
别名:
四氯化锡, 氯化高锡
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关于此项目
线性分子式:
SnCl4
化学文摘社编号:
分子量:
260.52
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
MDL number:
产品名称
氯化锡(IV) 溶液, 1.0 M in methylene chloride
InChI
1S/4ClH.Sn/h4*1H;/q;;;;+4/p-4
SMILES string
Cl[Sn](Cl)(Cl)Cl
InChI key
HPGGPRDJHPYFRM-UHFFFAOYSA-J
form
liquid
reaction suitability
core: tin
reagent type: catalyst
concentration
1.0 M in methylene chloride
density
1.419 g/mL at 25 °C
Quality Level
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Application
氯化锡（IV）溶液可用于聚砜的氯甲基化反应，以开发聚合物电解质膜。
General description
氯化锡（IV）具有路易斯酸的特征，并通常通过溶胶-凝胶法用于合成SnO2纳米颗粒。
Packaging
推荐将25毫升安全/密封™瓶作为一次性使用的瓶子。重复穿刺可能会导致产品性能下降。
Legal Information
Sure/Seal is a trademark of Sigma-Aldrich Co. LLC
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Carc. 2 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Central nervous system, Respiratory system
存储类别
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Phosphoric acid doped polysulfone membranes with aminopyridine pendant groups and imidazole cross-links.
Hink S, et al.
European Polymer Journal, 72(20), 102-113 (2015)
Solid-State and Solution Structural Study of Acetylacetone-Modified Tin (IV) Chloride Used as a Precursor of SnO2 Nanoparticles Prepared by a Sol- Gel Route.
Briois V, et al.
Chemistry of Materials, 16(20), 3885-3894 (2004)
Molecular addition compounds of tin (IV) chloride. I. Interaction with benzonitriles in benzene solution.
Brown TL and Kubota M
Journal of the American Chemical Society, 83(2), 331-334 (1961)
Gary B Evans et al.
The Journal of organic chemistry, 69(6), 2217-2220 (2004-04-03)
Promotion by Lewis acid of the addition of some aryllithiums to a carbohydrate-based imine, which has allowed a more facile synthesis of some imino-C-nucleoside analogues, is described. Use of the corresponding nitrone does not assist in some cases, but lithiated
Gerry A Griffith et al.
Journal of the American Chemical Society, 128(40), 13130-13141 (2006-10-05)
Difluorinated alkenoate ethyl 3,3-difluoro-2-(N,N-diethylcarbamoyloxy)-2-propenoate reacts rapidly and in high yield with furan and a range of substituted furans in the presence of a tin(IV) catalyst. Non-fluorinated congener 2-(N,N-diethylcarbamoyloxy)-2-propenoate fails to react at all under the same conditions. These reactions have
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