Trimethyltin hydroxide - ≥98% , CAS No.56-24-6

CAS: 56-24-6 Cat. No.: T283454 Fórmula: C₃H₁₀OSn Peso molecular: 180.80 Número CE: 677-697-9 PubChem CID: 6328620

GRADE & PURITY ≥98%

Synonyms

AT34590 | Trimethylstannanol | Trimethylstannyl hydroxide | AKOS025395384 | MFCD00013929 | Stannane, hydroxytrimethyl- | Trimethyltin hydroxide | Tin, hydroxytrimethyl- | AS-57825 | Hydroxytrimethylstannane | Trimethylhydroxytin | AI3-52035 | Tin, trimeth

Storage

Argon charged,Room temperature

Shipped In

Normal

Visão geral

Application：

Trimethyltin hydroxide is used in the synthesis of modified thymines, which is useful as inhibitors of RNase A. It is also used in the preparation of ketoheterocycle inhibitors of fatty acid amide inhibitors. It reacts with 2,2-disubstituted benzothiazolines to form trialkyltin derivatives of sulphur containing Schiff base complexes.

Begins to sublime at 80°C.Moisture and air sensitive. Incompatible with strong oxidizing agents and halogens.

Specifications

Sinónimos

AT34590 | Trimethylstannanol | Trimethylstannyl hydroxide | AKOS025395384 | MFCD00013929 | Stannane, hydroxytrimethyl- | Trimethyltin hydroxide | Tin, hydroxytrimethyl- | AS-57825 | Hydroxytrimethylstannane | Trimethylhydroxytin | AI3-52035 | Tin, trimeth

Especificações e pureza

≥98%

Condições de armazenamento de armazenamento

Argon charged,Room temperature

Enviado em

Normal

Pureza

≥98%

Nomes e identificadores

Pubchem Sid

504764069

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504764069

Sorrisos canónicos

C[Sn](C)C.O

InChIKey

UABRYPURASNHRO-UHFFFAOYSA-N

INCHI

1S/3CH3.H2O.Sn/h3*1H3;1H2;

SMILES isoméricas

C[Sn](C)C.O

PubChem CID

6328620

Peso molecular

180.80

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Classe Organo-post-transition metal compounds
      • Subclass Organotin compounds
        • Level5 Triorganotin compounds
          • Level6 Trialkyltins

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Classe: Organo-post-transition metal compounds
• Subclass: Organotin compounds
• Intermediate Tree Nodes: Triorganotin compounds
• Direct Parent: Trialkyltins
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkyltin - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as trialkyltins. These are triorganotin compounds where the tin atom is linked to exactly three alkyl groups.
• 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

Propriedades químicas e físicas

• Solubilidade: Soluble in water.
• Sensibilidade: Air sensitive；Moisture sensitive
• Ponto de fusão (°C): 114-118°C
• Peso molecular: 181.830 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 182.983 Da
• Monoisotopic Mass: 182.983 Da
• Topological Polar Surface Area: 1.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 11.600
• 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: 2

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