Gelest, Inc. 1,4-DIVINYL-1,1,4,4-TETRAMETHYL-1,4-DISILABUTANE SID4614.0

Description
Additional Properties Hydrolytic Sensitivity 1: no significant reaction with aqueous systems Application Intermediate for curare analogs.1 Potential vinyl nucleophile in cross-coupling reactions.2 Reference 1. Tacke, R. et al. Z. Naturforsch., B: Anorg. Chem., Org. Chem. 1982, 37B, 1461. 2. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety Packaging Under Nitrogen Alkenylsilane 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. 1,4-Divinyl-1,1,4,4- tetramethyl-1,4-disi labutane; Bis(ethenyldimethyls ilyl)ethane Potential vinyl donor in cross-coupling reactions Intermediate for curare analogs Potential vinyl nucleophile in cross-coupling 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
Datasheet
Description
Additional Properties Hydrolytic Sensitivity 1: no significant reaction with aqueous systems Application Intermediate for curare analogs.1 Potential vinyl nucleophile in cross-coupling reactions.2 Reference 1. Tacke, R. et al. Z. Naturforsch., B: Anorg. Chem., Org. Chem. 1982, 37B, 1461. 2. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety Packaging Under Nitrogen Alkenylsilane 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. 1,4-Divinyl-1,1,4,4- tetramethyl-1,4-disi labutane; Bis(ethenyldimethyls ilyl)ethane Potential vinyl donor in cross-coupling reactions Intermediate for curare analogs Potential vinyl nucleophile in cross-coupling 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
Datasheet

Suppliers

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1,4-DIVINYL-1,1,4,4-TETRAMETHYL-1,4-DISILABUTANE - SID4614.0 - Gelest, Inc.
Morrisville, PA, United States
1,4-DIVINYL-1,1,4,4-TETRAMETHYL-1,4-DISILABUTANE
SID4614.0
1,4-DIVINYL-1,1,4,4-TETRAMETHYL-1,4-DISILABUTANE SID4614.0
Additional Properties Hydrolytic Sensitivity 1: no significant reaction with aqueous systems Application Intermediate for curare analogs.1 Potential vinyl nucleophile in cross-coupling reactions.2 Reference 1. Tacke, R. et al. Z. Naturforsch., B: Anorg. Chem., Org. Chem. 1982, 37B, 1461. 2. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011. Safety Packaging Under Nitrogen Alkenylsilane 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. 1,4-Divinyl-1,1,4,4- tetramethyl-1,4-disi labutane; Bis(ethenyldimethyls ilyl)ethane Potential vinyl donor in cross-coupling reactions Intermediate for curare analogs Potential vinyl nucleophile in cross-coupling 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

Additional Properties


  • Hydrolytic Sensitivity 1: no significant reaction with aqueous systems
    Application
    Intermediate for curare analogs.1 Potential vinyl nucleophile in cross-coupling reactions.2
    Reference
    1. Tacke, R. et al. Z. Naturforsch., B: Anorg. Chem., Org. Chem. 1982, 37B, 1461. 2. Larson, G. L. “Silicon-Based Cross-Coupling Reagents” Gelest, Inc. 2011.
    Safety
  • Packaging Under Nitrogen
    Alkenylsilane 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.
    1,4-Divinyl-1,1,4,4-tetramethyl-1,4-disilabutane; Bis(ethenyldimethylsilyl)ethane
  • Potential vinyl donor in cross-coupling reactions
  • Intermediate for curare analogs
  • Potential vinyl nucleophile in cross-coupling 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
Supplier's Site Datasheet

Technical Specifications

  Gelest, Inc.
Product Category Organic Chemicals
Product Number SID4614.0
Product Name 1,4-DIVINYL-1,1,4,4-TETRAMETHYL-1,4-DISILABUTANE
Chemical Formula C 1 0 H 2 2 Si 2
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