Pack Size
10 g
50 g
2.5 kg

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

  • HMIS

  • Molecular Formula

  • Molecular Weight (g/mol)

  • Boiling Point (˚C/mmHg)

    130° / 0.2
  • Density (g/mL)

  • Refractive Index @ 20˚C


Additional Properties

  • Hydrolytic Sensitivity

    4: no reaction with water under neutral conditions
  • Application

    Transfers phenyl group to allylic acetates in Pd catalyzed reactions.1,2


    1. Stille, J. Angew. Chem., Int. Ed. Engl. 1986, 25, 508.
    2. Kosugi, M. Chem. Lett. 1987, 1237.


  • Packaging Under

  • 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.

    Phenyltri-n-butyltin; Phenyltri-n-butylstannane

  • Transfers phenyl group to allylic acetates in Pd catalyzed reactions
  • Stille Coupling phenylation reagent
  • Transfers phenyl group to allylaic acetates in Pd-catalyzed reactions
  • 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