Trimethylsulfonium hydroxide solution - 0.2mol/L in methanol , CAS No.17287-03-5

CAS: 17287-03-5 Cat. No.: T113600 Fórmula: C₃H₁₀OS Peso molecular: 94.18 Beilstein Registry Number: 3910286 Número CE: 628-493-3 PubChem CID: 11105313

GRADE & PURITY 0.2mol/L in methanol

Synonyms

DTXSID70938225 | Trimethylsulfoniumhydroxyd | UNII-835839L58Y | IODO-GLUTIONAL [WHO-DD] | Trimethylsulfanium Hydroxide | T1576 | trimethylsulfanium;hydroxide | 835839L58Y | MFCD00216756 | MDTPTXSNPBAUHX-UHFFFAOYSA-M | Sulfonium, trimethyl-, hydroxide | AI

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Visão geral

Trimethylsulfonium hydroxide (TMSH) is a methylating reagent. It can be prepared by dissolving trimethylsulfonium iodide in methanol and water solvent further treating with silver oxide.

Specifications

Sinónimos

DTXSID70938225 | Trimethylsulfoniumhydroxyd | UNII-835839L58Y | IODO-GLUTIONAL [WHO-DD] | Trimethylsulfanium Hydroxide | T1576 | trimethylsulfanium;hydroxide | 835839L58Y | MFCD00216756 | MDTPTXSNPBAUHX-UHFFFAOYSA-M | Sulfonium, trimethyl-, hydroxide | AI

Especificações e pureza

0.2mol/L in methanol

Condições de armazenamento de armazenamento

Store at -20°C

Enviado em

Ice chest + Ice pads

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Nomes e identificadores

• Pubchem Sid: 504766009
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504766009
• Sorrisos canónicos: C[S+](C)C.[OH-]
• IUPAC Name: trimethylsulfanium;hydroxide
• InChIKey: MDTPTXSNPBAUHX-UHFFFAOYSA-M
• INCHI: 1S/C3H9S.H2O/c1-4(2)3;/h1-3H3;1H2/q+1;/p-1
• SMILES isoméricas: C[S+](C)C.[OH-]
• WGK Alemanha: 2
• PubChem CID: 11105313
• Número UN: 3286
• Peso molecular: 94.18
• Beilstein: 3910286
• Reaxy-Rn: 3910286

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organic oxoanionic compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organic oxoanionic compounds
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Organic oxoanionic compounds
• Alternative Parents: Organosulfur compounds Organic salts Organic oxides Hydrocarbon derivatives Organic cations
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic oxide - Hydrocarbon derivative - Organic salt - Organosulfur compound - Organic hydroxide - Organic cation - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as organic oxoanionic compounds. These are organic compounds containing an oxoanion.
• 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

• Sensibilidade: heat sensitive
• Ponto de inflamação (°F): 11℃
• Ponto de inflamação (°C): 11℃
• Peso molecular: 94.180 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 94.0452 Da
• Monoisotopic Mass: 94.0452 Da
• Topological Polar Surface Area: 2.000 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 8.000
• 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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