N-METHYL-AZA-2,2,4-TRIMETHYLSILACYCLOPENTANE

Product Code: SIM6501.4
CAS No: 18387-19-4
SDS Sheets: EU | US
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18387-19-4
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25 g
$200.00
100 g
$297.00
2 kg
$3,920.00
16 kg
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160 kg
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Prices listed are EXW price (Morrisville, PA US) in USD. Prices vary depending on currency and Incoterms.

Product data and descriptions listed are typical values, not intended to be used as specification.

  • HMIS

    3-4-1-X
  • Molecular Formula

    C7H17NSi
  • Molecular Weight (g/mol)

    143.30
  • Purity (%)

    97%
  • TSCA

    Yes
  • Boiling Point (˚C/mmHg)

    137
  • Density (g/mL)

    0.813
  • Flash Point (˚C)

    14 °C
  • Refractive Index @ 20˚C

    1.4308

Additional Properties

  • Hydrolytic Sensitivity

    7: reacts slowly with moisture/water

    • Safety

  • Packaging Under

    Nitrogen

    • N-methyl-aza-2,2,4-trimethylsilacyclopentane

  • Amine functional silane coupling agent
  • Non-cross-linking cyclic azasilane
  • Employed in vapor phase modification of nanoparticles

    • Applied Technology

    A Mini Review Recent Advances in Surface Modification of Porous Silicon

    Silicon Chemistry, Applied Technology

    Cyclic Azasilanes and Cyclic Thiasilanes for Nano-Surface Modification

    How cyclic azasilanes and cyclic thiasilanes, a new class of silane coupling agents, modify nanoparticles and create nano-scale features.

    Silicon Chemistry, Applied Technology

    Cyclic Azasilanes: Volatile Coupling Agents for Nanotechnology – Arkles et al.

    Applied Technology

    Facile Surface Modification of Hydroxylated Silicon Nanostructures Using Heterocyclic Silanes

    Silicon Chemistry, Applied Technology

    Single-Molecule Orthogonal Double-Click Chemistry – Inorganic to Organic Nanostructure Transition – Arkles et al.

    Thiasilacyclopentane (TSCP) and azasilacyclopentane (ASCP) heteroatom cyclics reagents can be extended to “simultaneous doubleclicking” when both inorganic and organic substrates are present at the onset of the reaction. The simultaneous double-click depends on a first ring-opening click with an inorganic substrate that is complete in ~1 s at 30 °C and results in the reveal of a cryptic mercaptan or secondary amine group, which can then participate in a second click with an organic substrate.

    Applied Technology

    Surface-Triggered Tandem Coupling Reactions of Cyclic Azasilanes