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

CAS: 56-24-6 Cat. No.: T283454 Summenformel: C₃H₁₀OSn Molekulargewicht: 180.80 EG-Nummer: 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

Übersicht

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

Synonyme

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

Spezifikationen & Reinheit

≥98%

Storage

Argon charged,Room temperature

Verschickt in

Normal

Reinheit

≥98%

Namen und Kennungen

Pubchem Sid

504764069

Pubchem Sid Url

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

Kanonisches Lächeln

C[Sn](C)C.O

InChIKey

UABRYPURASNHRO-UHFFFAOYSA-N

INCHI

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

Isomere SMILES

C[Sn](C)C.O

PubChem CID

6328620

Molekulargewicht

180.80

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Klasse Organo-post-transition metal compounds
      • Subclass Organotin compounds
        • Ebene5 Triorganotin compounds
          • Ebene6 Trialkyltins

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in water.
• Empfindlichkeit: Air sensitive；Moisture sensitive
• Schmelzpunkt (°C): 114-118°C
• Molekulargewicht: 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

XLogP3