2-Amino-[1,2,4]triazolo[1,5-a]pyridin-6-ol hydrobromide
≥95%
- Product Code: 116372
CAS:
1092394-16-5
| Molecular Weight: | 231.05 g./mol | Molecular Formula: | C₆H₇BrN₄O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17014843 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their potential therapeutic activities. Researchers focus on its role in developing molecules with anti-inflammatory, anticancer, or antimicrobial properties. Its unique triazolopyridine structure makes it a valuable scaffold for designing drugs that target specific enzymes or receptors involved in disease pathways. Additionally, it is investigated for its potential use in creating fluorescent probes or imaging agents due to its aromatic and heterocyclic nature. Its hydrobromide form enhances solubility, making it easier to handle in experimental settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,617.00 |
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| 0.250 | 10-20 days | ฿6,894.00 |
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| 1.000 | 10-20 days | ฿17,235.00 |
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2-Amino-[1,2,4]triazolo[1,5-a]pyridin-6-ol hydrobromide
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various heterocyclic compounds, which are often explored for their potential therapeutic activities. Researchers focus on its role in developing molecules with anti-inflammatory, anticancer, or antimicrobial properties. Its unique triazolopyridine structure makes it a valuable scaffold for designing drugs that target specific enzymes or receptors involved in disease pathways. Additionally, it is investigated for its potential use in creating fluorescent probes or imaging agents due to its aromatic and heterocyclic nature. Its hydrobromide form enhances solubility, making it easier to handle in experimental settings.
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