2-(3-Carbamoyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylic acid
95%
- Product Code: 41465
Alias:
Febuxostat related substances
CAS:
1239233-86-3
| Molecular Weight: | 334.39 g./mol | Molecular Formula: | C₁₆H₁₈N₂O₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28138169 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both carbamoyl and carboxylic acid functional groups, makes it valuable for developing drugs targeting specific biological pathways. It is often employed in the creation of anti-inflammatory and analgesic medications, where its molecular framework aids in modulating enzyme activity or receptor interactions. Additionally, its thiazole ring contributes to its potential use in designing compounds with antimicrobial or antiviral properties. Researchers also explore its application in the development of small-molecule inhibitors for treating chronic diseases, leveraging its ability to interact with proteins or enzymes involved in disease progression.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to Off-White Solid |
| Purity | 94.5-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 G | 10-20 days | ฿28,800.00 |
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| 0.010 G | 10-20 days | ฿14,400.00 |
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2-(3-Carbamoyl-4-isobutoxyphenyl)-4-methylthiazole-5-carboxylic acid
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring both carbamoyl and carboxylic acid functional groups, makes it valuable for developing drugs targeting specific biological pathways. It is often employed in the creation of anti-inflammatory and analgesic medications, where its molecular framework aids in modulating enzyme activity or receptor interactions. Additionally, its thiazole ring contributes to its potential use in designing compounds with antimicrobial or antiviral properties. Researchers also explore its application in the development of small-molecule inhibitors for treating chronic diseases, leveraging its ability to interact with proteins or enzymes involved in disease progression.
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| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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