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Sigma-Aldrich 208930 Tin(IV) chloride 98% CAS No.: 7646-78-8 2 kg
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LB.SA.208930-2KG
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Synonym(s): Stannic chloride fuming Linear Formula: SnCl4 CAS Number: 7646-78-8 Molecular Weight: 260.52 EC Number: 231-588-9 MDL number: MFCD00011242 UNSPSC Code: 12352106 PubChem Substance ID: 24852219 NACRES: NA.22
| Sigma-Aldrich 208930 Tin(IV) chloride 98% CAS No.: 7646-78-8 2 kg |
| Synonym(s): Stannic chloride fuming Linear Formula: SnCl4 CAS Number: 7646-78-8 Molecular Weight: 260.52 EC Number: 231-588-9 MDL number: MFCD00011242 UNSPSC Code: 12352106 PubChem Substance ID: 24852219 NACRES: NA.22 |
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PROPERTIES
vapor density 9 (vs air)
Quality Level 200 vapor pressure 10 mmHg ( 10 °C) 18.6 mmHg ( 20 °C) 20 mmHg ( 22 °C) Assay 98% form liquid reaction suitability core: tin reagent type: Lewis acid reagent type: catalyst bp 114 °C (lit.) mp −33 °C (lit.) density 2.226 g/mL at 25 °C (lit.) SMILES string Cl[Sn](Cl)(Cl)Cl InChI 1S/4ClH.Sn/h4*1H;/q;;;;+4/p-4 InChI key HPGGPRDJHPYFRM-UHFFFAOYSA-J DESCRIPTION General description Stannic chloride (SnCl4) is a strong Lewis acid widely used as a promoter or catalyst in organic synthesis. It is soluble in most organic solvents.[1] Application Stannic chloride can be used to catalyze: - Cyclization of trans β-monocyclohomofarnesic acid to form norambreinolide.[2] - Formation of C-glycosides of aromatic compounds such as thiophene, naphthalene and phloroglucinol trimethyl ether.[3] - Formal [4+2] cycloaddition of 3-ethoxycyclobutanones and allyltrialkylsilanes to form 3-ethoxy-5-[(trialkylsilyl)methyl]cyclohexan-1-ones.[4] - Diastereoselective reaction of δ-alkoxyallylstannanes with aldehydes to form 1,5-diol derivatives.[5] Other applications of SnCl4: - The SnCl4-2,6-dialkoxyphenols complexes can catalyze cyclization of poylenes, such as 4-(homogeranyl)toluene to form trans-fused tricyclic compound.[6] - SnCl4 can act as a promoter during the reaction of ortho-aminobenzonitriles with β-ketoesters and β-enaminonitriles to form 4-aminoquinolines and 4-aminopyridines, respectively.[7] - SnCl4-silver perchlorate forms an effective catalytic system for the stereoselective of glycosylation 1-O-acetyl glucose.[8] |
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