4-(4-Methoxyphenyl)-1H-pyrazol-5-amine
95%
- Product Code: 210901
CAS:
93439-79-3
| Molecular Weight: | 189.21 g./mol | Molecular Formula: | C₁₀H₁₁N₃O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00141526 | |
| Melting Point: | 204～206 °C | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, light-proof storage, dry seal |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its ability to form hydrogen bonds and participate in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the creation of anti-inflammatory and analgesic agents owing to its pyrazole core, which is known for biological activity modulation. Its methoxyphenyl group contributes to improved solubility and metabolic stability in drug candidates. Additionally, it finds use in agrochemical research for designing new pesticides with selective activity.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $146.94 |
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| 250mg | 10-20 days | $248.26 |
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| 1g | 10-20 days | $490.15 |
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| 5g | 10-20 days | $1,804.09 |
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4-(4-Methoxyphenyl)-1H-pyrazol-5-amine
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of active pharmaceutical ingredients (APIs) due to its ability to form hydrogen bonds and participate in aromatic interactions, enhancing binding affinity to target proteins. Also employed in the creation of anti-inflammatory and analgesic agents owing to its pyrazole core, which is known for biological activity modulation. Its methoxyphenyl group contributes to improved solubility and metabolic stability in drug candidates. Additionally, it finds use in agrochemical research for designing new pesticides with selective activity.
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