N-[4-(3-Aminophenyl)-2-thiazolyl]acetamide
≥95%
- Product Code: 69602
CAS:
134812-30-9
| Molecular Weight: | 233.29 g./mol | Molecular Formula: | C₁₁H₁₁N₃OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01114798 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel therapeutic agents. Its structure, featuring both an aminophenyl group and a thiazole ring, makes it a valuable intermediate in the creation of compounds with potential biological activity. It is often explored for its role in developing drugs targeting inflammatory and infectious diseases, as the thiazole moiety is known to exhibit antimicrobial and anti-inflammatory properties. Additionally, its application extends to the study of enzyme inhibition, where it may serve as a scaffold for designing inhibitors of specific enzymes involved in disease pathways. Researchers also investigate its potential in cancer therapy, leveraging its ability to interact with cellular targets that regulate tumor growth.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow-white to Brown Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,070.00 |
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| 1.000 | 10-20 days | ฿5,990.00 |
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N-[4-(3-Aminophenyl)-2-thiazolyl]acetamide
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel therapeutic agents. Its structure, featuring both an aminophenyl group and a thiazole ring, makes it a valuable intermediate in the creation of compounds with potential biological activity. It is often explored for its role in developing drugs targeting inflammatory and infectious diseases, as the thiazole moiety is known to exhibit antimicrobial and anti-inflammatory properties. Additionally, its application extends to the study of enzyme inhibition, where it may serve as a scaffold for designing inhibitors of specific enzymes involved in disease pathways. Researchers also investigate its potential in cancer therapy, leveraging its ability to interact with cellular targets that regulate tumor growth.
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