Trihexylsilane - ≥95%(GC) , CAS No.2929-52-4

CAS: 2929-52-4 Cat. No.: T162511 Fórmula: C₁₈H₄₀Si Peso molecular: 284.6 Beilstein Registry Number: 4(4)3915 Número EC: 220-893-2 PubChem CID: 6327464

CALIDAD & PUREZA ≥95%(GC)

Synonyms

tri-n-Hexylsilane|trihexylsilicon|Silane, trihexyl-|trihexyl silane|Trihexylsilane

Storage

Room temperature

Shipped In

Normal

Descripción general

Reactant for: . Enantioselective Si-H insertion . Regio- and stereoselective oxidation into silanols . Asymmetric carbenoid insertion of diazoacetates into the silicon-hydrogen bond . Hydrosilylation of carbon dioxide Catalyst for hydrodefluorination leading to the synthesis of hydrocarbons

Especificaciones

Sinónimos

tri-n-Hexylsilane | trihexylsilicon | Silane, trihexyl- | trihexyl silane | Trihexylsilane

Especificaciones y pureza

≥95%(GC)

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥95%(GC)

Nombres e identificadores

Pubchem Sid

528769042

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/528769042

Sonrisas canónicas

CCCCCC[Si](CCCCCC)CCCCCC

InChIKey

ISPSHPOFLYFIRR-UHFFFAOYSA-N

INCHI

1S/C18H39Si/c1-4-7-10-13-16-19(17-14-11-8-5-2)18-15-12-9-6-3/h4-18H2,1-3H3

Isómeros SMILES

CCCCCC[Si](CCCCCC)CCCCCC

WGK Alemania

1

PubChem CID

6327464

Peso molecular

284.6

Beilstein

4(4)3915

Reaxy-Rn

1755830

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Hydrocarbon derivatives

• Kingdom: Organic compounds
• Superclass: Hydrocarbon derivatives
• Clase: Not available
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Hydrocarbon derivatives
• Alternative Parents: Organosilicon compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Hydrocarbon derivative - Organosilicon compound - Organic metalloid moeity - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as hydrocarbon derivatives. These are derivatives of hydrocarbons obtained by substituting one or more carbon atoms by an heteroatom. They contain at least one carbon atom and heteroatom.
• 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

• Sensibilidad: Moisture Sensitive
• Índice de refracción: 1.448(lit.)
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 62°C(lit.)
• Punto de ebullición (°C): 160.5-161 °C(lit.)
• Peso molecular: 283.600 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 15
• Exact Mass: 283.282 Da
• Monoisotopic Mass: 283.282 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 19
• Formal Charge: 0
• Complexity: 127.000
• 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: 1

XLogP3