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ETHYNYLTRIMETHYLSILANE, 98%
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ETHYNYLTRIMETHYLSILANE, 98%

CAS: 1066-54-2

Ref. 3H-SIE4904.0

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25gDescontinuado
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1.5kgDescontinuado
140kgDescontinuado

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Informação sobre produto

Nome:
ETHYNYLTRIMETHYLSILANE, 98%
Sinónimos:
  • TRIMETHYLSILYLACETYLENE
  • (Thrimethylsilyl)acetylene
  • (Trimethylsilanyl)acetylene
  • (Trimethylsilyl)acetylene
  • 1-(Trimethylsilyl)acetylene
  • 1-Trimethylsilylethyne
  • 2,2-Dimethyl-2-sila-3-butyne
  • Acetylene, Trimethylsilyl-
  • Acetylenyltrimethylsilane
  • Cetylene, Trimethylsilyl-
  • Ver mais sinónimos
  • 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
Descrição:

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

Aviso:
Os nossos productos estão destinados exclusivamente para uso em laboratório. Para qualquer outra aplicação, por favor entre em contacto.
Marca:
Gelest
Armazenamento a longo prazo:
Notas:

Propriedades químicas

Peso molecular:
98.22
Fórmula:
C5H10Si
Pureza:
98%
Cor/forma:
Straw Liquid
MDL:
Ponto de fusão:
Ponto de ebulição:
Ponto de inflamação:
Densidade:
Concentração:
EINECS:
Merck:
Código HS:

Informação sobre riscos

Número ONU:
EQ:
Classe:
Frases H:
Frases P:
Proibido de voar:
Informação sobre riscos:
Grupo de Embalagem:
LQ:

Consulta sobre o produto descontinuado: 3H-SIE4904.0 ETHYNYLTRIMETHYLSILANE, 98%

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