4,5-Dimethyl-3-(2-oxo-2-phenylethyl)thiazol-3-ium chloride
98%
- Product Code: 171426
CAS:
341028-37-3
| Molecular Weight: | 267.77 g./mol | Molecular Formula: | C₁₃H₁₄ClNOS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09027398 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used as a key intermediate in organic synthesis, particularly in the preparation of biologically active thiazole derivatives. It serves in the development of pharmaceuticals due to its ability to participate in cyclization and alkylation reactions. Commonly employed in the synthesis of fluorescent dyes and sensors, especially those targeting metal ions or biomolecules. Its quaternary thiazolium structure makes it valuable in catalyzing umpolung reactions, such as in Stetter or benzoin condensation-type transformations. Also explored in medicinal chemistry for antimicrobial and antitumor agent design.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,070.00 |
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| 1g | 10-20 days | ฿2,990.00 |
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| 5g | 10-20 days | ฿13,820.00 |
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4,5-Dimethyl-3-(2-oxo-2-phenylethyl)thiazol-3-ium chloride
Used as a key intermediate in organic synthesis, particularly in the preparation of biologically active thiazole derivatives. It serves in the development of pharmaceuticals due to its ability to participate in cyclization and alkylation reactions. Commonly employed in the synthesis of fluorescent dyes and sensors, especially those targeting metal ions or biomolecules. Its quaternary thiazolium structure makes it valuable in catalyzing umpolung reactions, such as in Stetter or benzoin condensation-type transformations. Also explored in medicinal chemistry for antimicrobial and antitumor agent design.
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