Triethoxymethylsilane - ≥98% , CAS No.2031-67-6

CAS: 2031-67-6 Cat. No.: T103634 Fórmula: C₇H₁₈O₃Si Peso molecular: 178.3 Beilstein Registry Number: 1742453 Número EC: 217-983-9 PubChem CID: 16241

CALIDAD & PUREZA ≥98%

Synonyms

MTES | Triethoxy(methyl)silane | Methyl triethoxysilane | Triethoxymethylsilane | Methyltriethoxysilane | Methaneorthosiliconic acid, triethyl ester | Silane, triethoxymethyl- | SILANE, METHYLTRIETHOXY- | Triethoxysilylmethane | Union carbide A-162

Storage

Room temperature,Argon charged,Desiccated

Shipped In

FedEx DG Service

Descripción general

Triethoxymethylsilane is an organosilane that can be used to prepare:
An oxidizing catalyst known with excellent features such as selectivity, stability, and recyclability.
A hydrogel heterogeneous platinum catalyst applicable in the chemoselective hydrogenation of nitroarenes

Especificaciones

Sinónimos

MTES | Triethoxy(methyl)silane | Methyl triethoxysilane | Triethoxymethylsilane | Methyltriethoxysilane | Methaneorthosiliconic acid, triethyl ester | Silane, triethoxymethyl- | SILANE, METHYLTRIETHOXY- | Triethoxysilylmethane | Union carbide A-162

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature,Argon charged,Desiccated

Enviado en

FedEx DG Service

Pureza

≥98%

Product Line

T103634-50ml

Nombres e identificadores

Pubchem Sid

504752737

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504752737

Sonrisas canónicas

CCO[Si](C)(OCC)OCC

IUPAC Name

triethoxy(methyl)silane

InChIKey

CPUDPFPXCZDNGI-UHFFFAOYSA-N

INCHI

1S/C7H18O3Si/c1-5-8-11(4,9-6-2)10-7-3/h5-7H2,1-4H3

Isómeros SMILES

CCO[Si](C)(OCC)OCC

WGK Alemania

3

RTECS

VV4640000

PubChem CID

16241

Número ONU

1993

Grupo de embalaje

III

Peso molecular

178.3

Beilstein

1742453

Reaxy-Rn

1742453

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Clase Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Alkoxysilanes
          • Level6 Trialkoxysilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Clase: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Alkoxysilanes
• Direct Parent: Trialkoxysilanes
• Alternative Parents: Silyl ethers Organoheterosilanes Organic metalloid salts Organooxygen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Trialkoxysilane - Silyl ether - Organoheterosilane - Organic metalloid salt - Organic oxygen compound - Hydrocarbon derivative - Organic salt - Organooxygen compound - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as trialkoxysilanes. These are organosilicon compounds with the general formula RO[Si](R')(OR'')OR''' (R-R''' = aliphatic organyl group).
• 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: Solubility in water: insoluble;Solubility in other solvents: soluble in most common organic solvents
• Sensibilidad: Moisture Sensitive
• Índice de refracción: 1.3835
• Punto de inflamación (°C): 23 °C
• Punto de ebullición (°C): 141-143 °C
• Peso molecular: 178.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 6
• Exact Mass: 178.103 Da
• Monoisotopic Mass: 178.103 Da
• Topological Polar Surface Area: 27.700 Ų
• Heavy Atom Count: 11
• Formal Charge: 0
• Complexity: 80.700
• 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: 1

XLogP3