1,2-Bis(triethoxysilyl)ethane - ≥96% , CAS No.16068-37-4

CAS: 16068-37-4 Cat. No.: W132160 Peso molecular: 354.59 Número EC: 240-212-2 PubChem CID: 85266

GRADE & PURITY ≥96%

Synonyms

Ethylenebis(triethoxysilane) | 4,4,7,7-Tetraethoxy-3,8-dioxa-4,7-disiladecane | 1,2-Bis(triethoxysilyl)ethane | 1,2-(Triethoxysilyl)ethane

Storage

Argon charged,Room temperature

Shipped In

Normal

Descripción general

1,2-Bis(triethoxysilyl)ethane (BTESE) is a silsesquioxane precursor which is mainly used in the preparation of mesoporous organic materials. It can tune silica networks which makes them useful in applications related to molecular separation. 
1,2-bis(triethoxysilyl)ethane is a non-functional silane and a double trialkoxysilyl precursor.

Specifications

Sinónimos

Ethylenebis(triethoxysilane) | 4, 4, 7, 7-Tetraethoxy-3, 8-dioxa-4, 7-disiladecane | 1, 2-Bis(triethoxysilyl)ethane | 1, 2-(Triethoxysilyl)ethane

Especificaciones y pureza

≥96%

Condiciones de almacenamiento de almacenamiento

Argon charged, Room temperature

Enviado en

Normal

Pureza

≥96%

Nombres e identificadores

• Pubchem Sid: 488186308
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186308
• Sonrisas canónicas: CCO[Si](CC[Si](OCC)(OCC)OCC)(OCC)OCC
• IUPAC Name: triethoxy(2-triethoxysilylethyl)silane
• InChIKey: IZRJPHXTEXTLHY-UHFFFAOYSA-N
• INCHI: 1S/C14H34O6Si2/c1-7-15-21(16-8-2,17-9-3)13-14-22(18-10-4,19-11-5)20-12-6/h7-14H2,1-6H3
• Isómeros SMILES: CCO[Si](CC[Si](OCC)(OCC)OCC)(OCC)OCC
• WGK Alemania: 3
• RTECS: JG7755000
• PubChem CID: 85266
• Peso molecular: 354.59

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: Soluble in alcohol, aromatic and aliphatic hydrocarbons. Hydrolyzes with water.
• Sensibilidad: Hygroscopic
• Índice de refracción: 1.41
• Rotación específica [α]: 1.41
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 119 °C
• Peso molecular: 354.590 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 15
• Exact Mass: 354.189 Da
• Monoisotopic Mass: 354.189 Da
• Topological Polar Surface Area: 55.400 Ų
• Heavy Atom Count: 22
• Formal Charge: 0
• Complexity: 208.000
• 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

Referencias

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