Pack Size
Quantity
Price
 
10 g
$59.00

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

  • HMIS

    3-1-0-X
  • Molecular Formula

    C16H30SSn
  • Molecular Weight (g/mol)

    373.17
  • Purity (%)

    95%
  • Boiling Point (˚C/mmHg)

    155° / 0.1
  • Density (g/mL)

    1.175
  • Flash Point (˚C)

    106°C (223°F)
  • Refractive Index @ 20˚C

    1.5180

Safety

  • Packaging Under

    Nitrogen
  • Organotin Cross-Coupling Agent

    The cross-coupling reaction is a highly useful methodology for the formation of carbon-carbon bonds. It involves two reagents, with one typically being a suitable organometallic reagent - the nucleophile - and the other a suitable organic substrate, normally an unsaturated halide, tosylate or similar - the electrophile.

    2-Thienyltri-n-butyltin; 2-Thiophenyltri-n-butylstannane

  • Stille Coupling for formation of 2-thienyl derivatives
  • Extensive review of silicon based cross-coupling agents: Denmark, S. E. et al. "Organic Reactions, Volume 75" Denmark, S. E. ed., John Wiley and Sons, 233, 2011
  • Metal-Organic Chemistry, Articles

    Silicon Chemistry, Articles

    Silicon-Based Formation of Carbon-Carbon Bonds – Larson

    Hatanaka and Hiyama first reported the palladium-catalyzed, fluoride-promoted reaction of aryl, alkenyl, allyl, and ethynyltrimethylsilanes with aryl, vinil and allyl halides to form the respective cross-coupled products