1-[(Trimethylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one
≥98%
- Product Code: 78340
CAS:
181934-29-2
| Molecular Weight: | 344.22 g./mol | Molecular Formula: | C₁₂H₁₃IO₂Si |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of alkynes into various molecular frameworks. Its unique structure allows it to act as a stable and efficient source of ethynyl groups, which are crucial in constructing complex organic molecules. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its trimethylsilyl group provides protection for the alkyne moiety, ensuring controlled reactivity during multi-step synthetic processes. This reagent is also employed in the development of novel polymers and functionalized materials, where precise alkyne incorporation is essential for tailoring properties such as conductivity, flexibility, and chemical stability.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Slightly pale reddish yellow Crystal - Powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $66.45 |
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| 1.000 | 10-20 days | $234.64 |
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1-[(Trimethylsilyl)ethynyl]-1,2-benziodoxol-3(1H)-one
This chemical is primarily utilized in organic synthesis as a versatile reagent for the introduction of alkynes into various molecular frameworks. Its unique structure allows it to act as a stable and efficient source of ethynyl groups, which are crucial in constructing complex organic molecules. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its trimethylsilyl group provides protection for the alkyne moiety, ensuring controlled reactivity during multi-step synthetic processes. This reagent is also employed in the development of novel polymers and functionalized materials, where precise alkyne incorporation is essential for tailoring properties such as conductivity, flexibility, and chemical stability.
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