Tin(IV) acetate - ≥95% , CAS No.2800-96-6

CAS: 2800-96-6 Cat. No.: T303317 Summenformel: C₈H₁₂O₈Sn Molekulargewicht: 354.89 EG-Nummer: 628-765-1 PubChem CID: 9863446

GRADE & PURITY ≥95%

Synonyms

tin(4+);tetraacetate | Tin(IV) acetate | DTXSID10432055 | tin-(IV)-acetate | AKOS025293663 | YJGJRYWNNHUESM-UHFFFAOYSA-J | tin (IV) acetate | Tetraacetoxytin; Tinacetate | TETRAACETOXYTIN | A876810 | FT-0705097

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Übersicht

Tin(IV) acetate is used to prepare tin-based oxides (Sn-Zn-P-O), which is a negative electrodes for rechargeable lithium batteries.

Specifications

Synonyme

tin(4+);tetraacetate | Tin(IV) acetate | DTXSID10432055 | tin-(IV)-acetate | AKOS025293663 | YJGJRYWNNHUESM-UHFFFAOYSA-J | tin (IV) acetate | Tetraacetoxytin; Tinacetate | TETRAACETOXYTIN | A876810 | FT-0705097

Spezifikationen & Reinheit

≥95%

Storage

Room temperature,Argon charged,Desiccated

Verschickt in

Normal

Reinheit

≥95%

Namen und Kennungen

Pubchem Sid

504765004

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504765004

Kanonisches Lächeln

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Sn+4]

IUPAC Name

tin(4+);tetraacetate

InChIKey

YJGJRYWNNHUESM-UHFFFAOYSA-J

INCHI

1S/4C2H4O2.Sn/c4*1-2(3)4;/h4*1H3,(H,3,4);/q;;;;+4/p-4

Isomere SMILES

CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].CC(=O)[O-].[Sn+4]

PubChem CID

9863446

Molekulargewicht

354.89

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Klasse Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Ebene5 Carboxylic acid salts
          • Ebene6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Klasse: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Monocarboxylic acids and derivatives Carboxylic acids Organic tin salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Acetate salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic tin salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Beschreibung: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in acetone and benzene.
• Empfindlichkeit: Moisture sensitive
• Schmelzpunkt (°C): 232-233 °C (lit.)
• Molekulargewicht: 354.890 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 0
• Exact Mass: 355.955 Da
• Monoisotopic Mass: 355.955 Da
• Topological Polar Surface Area: 161.000 Ų
• Heavy Atom Count: 17
• Formal Charge: 0
• Complexity: 25.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 5

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