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

CAS: 56-24-6 Cat. No.: T283454 Peso molecular: 180.80 Número EC: 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

Descripción general

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

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504764069
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764069
• Sonrisas canónicas: C[Sn](C)C.O
• InChIKey: UABRYPURASNHRO-UHFFFAOYSA-N
• INCHI: 1S/3CH3.H2O.Sn/h3*1H3;1H2
• Isómeros SMILES: C[Sn](C)C.O
• PubChem CID: 6328620
• Peso molecular: 180.80

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: 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
• Descripción: 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water.
• Sensibilidad: Air sensitive；Moisture sensitive
• Punto de fusión (°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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