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30-2490

Sigma-Aldrich

Zinn(II)-chlorid Dihydrat

SAJ first grade, ≥90.0%

Synonym(e):

Stannochlorid

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About This Item

Lineare Formel:
SnCl2 · 2H2O
CAS-Nummer:
10025-69-1
Molekulargewicht:
225.65
MDL-Nummer:
MFCD00149863
UNSPSC-Code:
12352302
PubChem Substanz-ID:
329753356

Qualität

SAJ first grade

Assay

≥90.0%

Form

solid

Eignung der Reaktion

reagent type: catalyst
core: tin

Verfügbarkeit

available only in Japan

bp

652 °C (lit.)

mp (Schmelzpunkt)

37-38 °C (dec.) (lit.)

Lagertemp.

2-8°C

SMILES String

O.O.Cl[SnH2]Cl

InChI

1S/2ClH.2H2O.Sn/h2*1H;2*1H2;/q;;;;+2/p-2

InChIKey

FWPIDFUJEMBDLS-UHFFFAOYSA-L

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Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1 - STOT RE 2 Oral - STOT SE 3

Zielorgane

Cardio-vascular system, Respiratory system

Lagerklassenschlüssel

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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David J Hallett et al.
Organic & biomolecular chemistry, 10(30), 6130-6158 (2012-04-20)
Reactions of the allyltin trichloride 45 generated from (4S)-4-benzyloxypent-2-enyl(tributyl)stannane 1 with imines prepared from glyoxylates proceed with useful levels of 1,5-stereocontrol in favour of (4E)-2,6-anti-2-(alkylamino)-6-benzyloxyhept-4-enoates 49. This stereoselectivity, controlled by the chirality of the stannane, dominates over any intrinsic stereochemical
Lindsay A Hobson et al.
Organic & biomolecular chemistry, 10(37), 7510-7526 (2012-08-14)
Transmetallation of the 5-benzyloxy-4-methylpent-2-en-1-yl(tributyl)- and -(triphenyl)stannanes 1 and 8 using tin(iv) chloride generates an allyltin trichloride that reacts with aldehydes to give (Z)-1,5-anti-6-benzyloxy-5-methylhex-3-en-1-ols 2. The allyltin trichloride believed to be the key intermediate in these reactions has been trapped by
Caitian Gao et al.
Nanoscale, 4(11), 3475-3481 (2012-05-11)
A high-efficiency photoelectrode for dye-sensitized solar cells (DSSCs) should combine the advantageous features of fast electron transport, slow interfacial electron recombination and large specific surface area. However, these three requirements usually cannot be achieved simultaneously in the present state-of-the-art research.
Liyan Zheng et al.
Dalton transactions (Cambridge, England : 2003), 41(5), 1630-1634 (2011-12-08)
It was found that stannous chloride (SnCl(2)), as a popular inorganic reducing reagent, could obviously enhance the electrochemiluminescence (ECL) of tris(2,2'-bipyridyl) ruthenium(II) (Ru(bpy)(3)(2+)) in aqueous solution. Some factors affecting the ECL reactions between Ru(bpy)(3)(2+) and Sn(2+), including pH, concentrations of
Matthew Currie et al.
Inorganic chemistry, 52(4), 1710-1721 (2012-06-09)
The anionic speciation of chlorostannate(II) ionic liquids, prepared by mixing 1-alkyl-3-methylimidazolium chloride and tin(II) chloride in various molar ratios, χ(SnCl2), was investigated in both solid and liquid states. The room temperature ionic liquids were investigated by (119)Sn NMR spectroscopy, X-ray
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