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ETHYNYLTRIMETHYLSILANE, 98%
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ETHYNYLTRIMETHYLSILANE, 98%

CAS: 1066-54-2

Ref. 3H-SIE4904.0

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Estimated delivery in United States, on Tuesday 14 Jan 2025

Product Information

Name:
ETHYNYLTRIMETHYLSILANE, 98%
Synonyms:
  • TRIMETHYLSILYLACETYLENE
  • (Thrimethylsilyl)acetylene
  • (Trimethylsilanyl)acetylene
  • (Trimethylsilyl)acetylene
  • 1-(Trimethylsilyl)acetylene
  • 1-Trimethylsilylethyne
  • 2,2-Dimethyl-2-sila-3-butyne
  • Acetylene, Trimethylsilyl-
  • Acetylenyltrimethylsilane
  • Cetylene, Trimethylsilyl-
  • See more synonyms
  • Ethinyltrimethylsilane
  • Ethynyltrimethylsilane
  • Ilane, Ethynyltrimethyl-
  • Ilane, Trimethyl-, Ethynyl-
  • Ms Acetylene
  • Rimethylethynylsilane
  • Rimethylsilylacetylene,Min
  • Silane, ethynyltrimethyl-
  • TMS acetylene
  • Thinyltrimethylsilane
  • Thyne,-Trimethylsilyl
  • Thynyltrimethyl-Silan
  • Thynyltrimethylsilane
  • Thynyltrimethylsilane, Wacker-Quality
  • Timethylsilylacetylene
  • Tmsa
  • Trimethyl silyl acetylene
  • Trimethylethynylsilane
  • Trimethylsil yace tylene
  • Trimethylsilanylethyne
  • Trimethylsilyl)ethyne
  • Trimethylsilylacetylen
  • Trimethylsilylethyne
  • Trimetilsililacetileno
Description:

Alkynylsilane 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.
Ethynyltrimethylsilane; Trimethylsilylacetylene
Vapor pressure, 20 °C: 214 mmUseful in Sonogashira reactions with differentiated reactivity at each terminus leading to unsymmetrical diaryl acetylenesReacts with aryl aldehydes to give diethynylmethanes (1,4-diynes)Doped polymer films are conductiveEthynylates aromatic compoundsPrecursor to trimethylsilylethynyl copper reagentLithiated derivative (n-BuLi treatment) reacts with halotriazines to produce monomersEmployed in ortho ethenylation of phenolsUndergoes Diels-Alder reactions with butadienesConverts imines to propargyl aminesForms propargylic amines from aldehydes and amines in aqueous systemRegioselectively forms either regioisomeric enyne upon addition to propargyl amines depending on catalyst employedReacts with aryl aldehydes to form diethynylmethane derivativesUseful in the preparation of unsymmetrical diarylacetylenesExtensive 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

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Gelest
Long term storage:
Notes:

Chemical properties

Molecular weight:
98.22
Formula:
C5H10Si
Purity:
98%
Color/Form:
Straw Liquid
MDL:
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EINECS:
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Hazard Info

UN Number:
EQ:
Class:
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