Pack Size
Quantity
Price
 
5 g
$80.00

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

  • HMIS

    3-2-0-X
  • Molecular Formula

    C12H24Sn
  • Molecular Weight (g/mol)

    287.01
  • TSCA

    No
  • Boiling Point (˚C/mmHg)

    60° / 0.4
  • Density (g/mL)

    1.122
  • Refractive Index @ 20˚C

    1.4749

Additional Properties

  • Hydrolytic Sensitivity

    1: no significant reaction with aqueous systems
  • 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.

    Divinyldi-n-butyltin; Dibutyldivinyltin; Dibutyldivinylstannane; Dibutyldiethenylstannane

  • Stille Coupling vinylation reagent
  • 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