2-((tert-Butoxycarbonyl)amino)-4-methylthiazole-5-carboxylic acid
97%
- Product Code: 41177
CAS:
302963-94-6
| Molecular Weight: | 258.2900 g./mol | Molecular Formula: | C₁₀H₁₄N₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01631191 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.359g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of thiazole-based drugs, which are known for their diverse biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. The tert-butoxycarbonyl (Boc) protecting group in its structure allows for selective reactions during multi-step organic synthesis, making it valuable in medicinal chemistry. Additionally, it is employed in the preparation of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,061.00 |
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2-((tert-Butoxycarbonyl)amino)-4-methylthiazole-5-carboxylic acid
This chemical is primarily utilized in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of thiazole-based drugs, which are known for their diverse biological activities, including antimicrobial, anti-inflammatory, and anticancer properties. The tert-butoxycarbonyl (Boc) protecting group in its structure allows for selective reactions during multi-step organic synthesis, making it valuable in medicinal chemistry. Additionally, it is employed in the preparation of peptidomimetics and other bioactive molecules, contributing to advancements in drug discovery and development.
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