2-(2-(5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide
98%
- Product Code: 41310
CAS:
489408-02-8
| Molecular Weight: | 386.3900 g./mol | Molecular Formula: | C₁₆H₁₇F₃N₄O₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02053612 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting specific enzyme pathways, particularly those involved in inflammatory and metabolic disorders. Its structural features, including the pyrazole and tetrahydrobenzo[b]thiophene moieties, make it a valuable scaffold for designing inhibitors or modulators of protein interactions. Researchers also explore its potential in creating novel therapeutics for conditions such as cancer, autoimmune diseases, and neurological disorders due to its ability to interact with diverse biological targets. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, making it a promising candidate for drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $14.04 |
+
-
|
2-(2-(5-Methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. It is often employed in the development of pharmaceutical agents targeting specific enzyme pathways, particularly those involved in inflammatory and metabolic disorders. Its structural features, including the pyrazole and tetrahydrobenzo[b]thiophene moieties, make it a valuable scaffold for designing inhibitors or modulators of protein interactions. Researchers also explore its potential in creating novel therapeutics for conditions such as cancer, autoimmune diseases, and neurological disorders due to its ability to interact with diverse biological targets. Additionally, its trifluoromethyl group enhances its metabolic stability and binding affinity, making it a promising candidate for drug discovery programs.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
$0.00
$0.00
Total :