5-Amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazole-3-thiol
99%
- Product Code: 48642
CAS:
878671-96-6
| Molecular Weight: | 282.36 g./mol | Molecular Formula: | C₁₅H₁₄N₄S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 475.167°C | |
| Density: | 1.52 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a triazole ring and a cyclopropylnaphthalene moiety, makes it valuable for designing compounds with potential antimicrobial, antifungal, or anticancer properties. Researchers explore its derivatives for their ability to inhibit specific pathways or proteins involved in disease progression. Additionally, its thiol group allows for further chemical modifications, enhancing its versatility in creating novel therapeutic agents.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow Solid |
| PURITY | 98.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | £48.85 |
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| 1.000 | 10-20 days | £96.69 |
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5-Amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazole-3-thiol
This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structure, featuring a triazole ring and a cyclopropylnaphthalene moiety, makes it valuable for designing compounds with potential antimicrobial, antifungal, or anticancer properties. Researchers explore its derivatives for their ability to inhibit specific pathways or proteins involved in disease progression. Additionally, its thiol group allows for further chemical modifications, enhancing its versatility in creating novel therapeutic agents.
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