6-Chloro-3-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridine
97%
- Product Code: 49741
CAS:
1431720-68-1
| Molecular Weight: | 221.5670 g./mol | Molecular Formula: | C₇H₃ClF₃N₃ |
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| EC Number: | MDL Number: | MFCD28677466 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrazolo[4,3-c]pyridine core with chloro and trifluoromethyl substituents, makes it a valuable building block for developing pharmaceutical agents. It is often employed in the creation of compounds targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antiviral drugs. Researchers leverage its chemical framework to design and optimize drug candidates with enhanced potency, selectivity, and metabolic stability. Additionally, its trifluoromethyl group contributes to improved lipophilicity and bioavailability, making it a versatile component in drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,895.00 |
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6-Chloro-3-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridine
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrazolo[4,3-c]pyridine core with chloro and trifluoromethyl substituents, makes it a valuable building block for developing pharmaceutical agents. It is often employed in the creation of compounds targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antiviral drugs. Researchers leverage its chemical framework to design and optimize drug candidates with enhanced potency, selectivity, and metabolic stability. Additionally, its trifluoromethyl group contributes to improved lipophilicity and bioavailability, making it a versatile component in drug discovery efforts.
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