3-(1H-1,2,3-triazol-4-yl) pyridine
99%
- Product Code: 99286
CAS:
120241-79-4
Molecular Weight: | 146.15 g./mol | Molecular Formula: | C₇H₆N₄ |
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EC Number: | MDL Number: | MFCD25956467 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of various biologically active molecules. Its structure, featuring a triazole ring fused with a pyridine ring, makes it a valuable scaffold in drug discovery, particularly for designing compounds with potential antiviral, anticancer, or anti-inflammatory properties. Researchers often incorporate it into larger molecules to enhance binding affinity or modulate pharmacokinetic properties. Additionally, it finds applications in material science, where it is used to develop functional materials with specific electronic or optical properties. Its versatility also extends to coordination chemistry, where it acts as a ligand in the formation of metal complexes for catalytic or sensing applications.
Product Specification:
Test | Specification |
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APPEARANCE | SOLID |
PURITY | 98.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.005 | 10-20 days | £209.05 |
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3-(1H-1,2,3-triazol-4-yl) pyridine
This compound is primarily utilized in the field of medicinal chemistry as a building block for the synthesis of various biologically active molecules. Its structure, featuring a triazole ring fused with a pyridine ring, makes it a valuable scaffold in drug discovery, particularly for designing compounds with potential antiviral, anticancer, or anti-inflammatory properties. Researchers often incorporate it into larger molecules to enhance binding affinity or modulate pharmacokinetic properties. Additionally, it finds applications in material science, where it is used to develop functional materials with specific electronic or optical properties. Its versatility also extends to coordination chemistry, where it acts as a ligand in the formation of metal complexes for catalytic or sensing applications.
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