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Merck
CN

14520

Tin(IV) chloride

fuming, ≥99%

Synonym(s):

Stannic chloride

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About This Item

Linear Formula:
SnCl4
CAS Number:
7646-78-8
Molecular Weight:
260.52
UNSPSC Code:
12352100
PubChem Substance ID:
329750518
EC Number:
231-588-9
MDL number:
MFCD00011242

Key Documents

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Quality Level

100

assay

≥99%

reaction suitability

reagent type: catalyst
core: tin

density

2.217 g/mL at 20 °C (lit.)

anion traces

sulfate (SO42-): ≤100 mg/kg

cation traces

As: ≤50 mg/kg, Fe: ≤10 mg/kg

SMILES string

Cl[Sn](Cl)(Cl)Cl

InChI

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

InChI key

HPGGPRDJHPYFRM-UHFFFAOYSA-J

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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 1

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

flash_point_f

No data available

flash_point_c

No data available

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
7032A
61150
51290
80250
60320

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Yasuyuki Kita et al.
The Journal of organic chemistry, 71(14), 5191-5197 (2006-07-01)
The Lewis acid-promoted rearrangement of 2,2,3,3-tetrasubstituted 2,3-epoxy alcohols with several kinds of protecting groups was investigated. When SnCl4 is used as a Lewis acid, the reaction proceeds in a regio- and stereo-controlled manner to afford two types of carbonyl compounds
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
Raquel Coronel et al.
Molecular neurobiology, 56(2), 1248-1261 (2018-06-09)
Amyloid precursor protein (APP) is implicated in neural development as well as in the pathology of Alzheimer's disease (AD); however, its biological function still remains unclear. It has been reported that APP stimulates the proliferation and neuronal differentiation of neural
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
Colin O'Brien et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 13(3), 902-909 (2006-11-07)
The reaction of silylated nucleophiles with 6,1-anhydroglucopyranuronic acid (glucuronic acid 6,1-lactones) catalysed by tin(IV) chloride provides 1,2-trans or 1,2-cis (deoxy)glycosides in a manner dependent on the donor structure. The alpha-glycoside was obtained for reactions of the donor with the 2-acyl
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