2-(Trimethylsilyl)thiazole
96%
- Product Code: 115853
Alias:
2-(Trimethylsilyl)thiazole ;2-(Trimethylsilyl)thiazole
CAS:
79265-30-8
| Molecular Weight: | 157.31 g./mol | Molecular Formula: | C₆H₁₁NSSi |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00066274 | |
| Melting Point: | Boiling Point: | 56-57 °C10 mm Hg(lit.) | |
| Density: | 0.985 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Used in organic synthesis as a building block for the preparation of more complex thiazole derivatives. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of compounds with potential antimicrobial, antiviral, or anticancer properties. Additionally, it is utilized in the production of agrochemicals, where thiazole-based compounds are known for their pesticidal and herbicidal activities. Its trimethylsilyl group enhances reactivity, making it a valuable reagent in nucleophilic substitution and coupling reactions.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 96-100 |
| Refractive Index N20/D | 1.495-1.5 |
| Specific Gravity (20/20 Degree Celsius) | 0.985-1.99 |
| Appearance | Colorless To Yellow Viscous Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,151.00 |
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| 5.000 | 10-20 days | ฿7,902.00 |
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| 25.000 | 10-20 days | ฿33,831.00 |
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2-(Trimethylsilyl)thiazole
Used in organic synthesis as a building block for the preparation of more complex thiazole derivatives. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of compounds with potential antimicrobial, antiviral, or anticancer properties. Additionally, it is utilized in the production of agrochemicals, where thiazole-based compounds are known for their pesticidal and herbicidal activities. Its trimethylsilyl group enhances reactivity, making it a valuable reagent in nucleophilic substitution and coupling reactions.
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