1,6-Bis(Trichlorosilyl)Hexane - ≥97% , CAS No.13083-94-8

CAS: 13083-94-8 Cat. No.: B302347 Molecular Weight: 353.03 EC Number: 235-994-7

GRADE & PURITY ≥97%

Synonyms

Silane, 1,6-hexanediylbis(trichloro- | Trichloro[6-(trichlorosilyl)hexyl]silane | Silane, 1,6-hexanediylbis[trichloro- | AS-80176 | Trichloro[6-(trichlorosilyl)hexyl]silane # | ICJGKYTXBRDUMV-UHFFFAOYSA-N | EINECS 235-994-7 | Silane, 1,6-hexanediylbis*tri

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

Product Application:

1,6-Bis(trichlorosilyl)hexane is a silane based cross-linking agent that can be used in the synthesis of polymeric blended films. These films are majorly utilized as dielectrics for applications in organic electronic based devices such as organic field effect transistors (OFETs) and organic thin film transistors (OTFTs).

Specifications

Synonyms

Silane, 1, 6-hexanediylbis(trichloro- | Trichloro[6-(trichlorosilyl)hexyl]silane | Silane, 1, 6-hexanediylbis[trichloro- | AS-80176 | Trichloro[6-(trichlorosilyl)hexyl]silane # | ICJGKYTXBRDUMV-UHFFFAOYSA-N | EINECS 235-994-7 | Silane, 1, 6-hexanediylbis*tri

Specifications & Purity

≥97%

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488186153
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488186153
• Canonical Smiles: C(CCC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl
• IUPAC Name: trichloro(6-trichlorosilylhexyl)silane
• InChIKey: ICJGKYTXBRDUMV-UHFFFAOYSA-N
• INCHI: 1S/C6H12Cl6Si2/c7-13(8,9)5-3-1-2-4-6-14(10,11)12/h1-6H2
• Isomeric SMILES: C(CCC[Si](Cl)(Cl)Cl)CC[Si](Cl)(Cl)Cl
• Molecular Weight: 353.03
• Reaxy-Rn: 1768655
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1768655&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organometallic compounds
    • Class Organometalloid compounds
      • Subclass Organosilicon compounds
        • Level5 Organoheterosilanes
          • Level6 Organochlorosilanes

• Kingdom: Organic compounds
• Superclass: Organometallic compounds
• Class: Organometalloid compounds
• Subclass: Organosilicon compounds
• Intermediate Tree Nodes: Organoheterosilanes
• Direct Parent: Organochlorosilanes
• Alternative Parents: Organic metalloid salts Alkylhalosilanes Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organochlorosilane - Organic metalloid salt - Alkylhalosilane - Hydrocarbon derivative - Organic salt - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as organochlorosilanes. These are organosilicon compounds where the tetravalent silicon atom is linked to one or more chlorine atoms.
• 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

Chemical and Physical Properties

• Sensitivity: Moisture Sensitive
• Refractive Index: 1.48
• Flash Point(°C): 75 °C
• Boil Point(°C): 148°
• Molecular Weight: 353.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 5
• Exact Mass: 351.858 Da
• Monoisotopic Mass: 349.861 Da
• Topological Polar Surface Area: 0.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 133.000
• 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

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