Phenyl[4-(trimethylsilyl)thiophen-3-yl]iodonium Trifluoromethanesulfonate
≥95%
- Product Code: 65864
CAS:
175224-35-8
| Molecular Weight: | 508.38 g./mol | Molecular Formula: | C₁₄H₁₆F₃IO₃S₂Si |
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| Melting Point: | 172°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis as a highly efficient reagent for introducing the phenyl group into various substrates. Its application is particularly significant in the field of photochemistry, where it serves as a photoacid generator (PAG) in photoresist formulations for advanced lithography processes in semiconductor manufacturing. The compound's ability to release strong acids upon exposure to light makes it invaluable in creating high-resolution patterns on silicon wafers, essential for producing microelectronic devices. Additionally, it is employed in the synthesis of complex organic molecules, where its reactivity facilitates the formation of carbon-carbon and carbon-heteroatom bonds, aiding in the development of pharmaceuticals and fine chemicals. Its stability and precise reactivity under controlled conditions make it a versatile tool in both industrial and research settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿15,810.00 |
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Phenyl[4-(trimethylsilyl)thiophen-3-yl]iodonium Trifluoromethanesulfonate
This chemical is primarily used in organic synthesis as a highly efficient reagent for introducing the phenyl group into various substrates. Its application is particularly significant in the field of photochemistry, where it serves as a photoacid generator (PAG) in photoresist formulations for advanced lithography processes in semiconductor manufacturing. The compound's ability to release strong acids upon exposure to light makes it invaluable in creating high-resolution patterns on silicon wafers, essential for producing microelectronic devices. Additionally, it is employed in the synthesis of complex organic molecules, where its reactivity facilitates the formation of carbon-carbon and carbon-heteroatom bonds, aiding in the development of pharmaceuticals and fine chemicals. Its stability and precise reactivity under controlled conditions make it a versatile tool in both industrial and research settings.
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