2-Amino-8-bromo[1,2,4]triazolo[1,5-a]pyridine
97%
- Product Code: 116361
CAS:
1124382-72-4
| Molecular Weight: | 213.04 g./mol | Molecular Formula: | C₆H₅BrN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16658939 | |
| Melting Point: | Boiling Point: | ||
| Density: | 2.098 g/cm3 | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural framework is often incorporated into compounds being studied for their potential as therapeutic agents, such as anxiolytics, anticonvulsants, or antipsychotics. Additionally, it is used in organic chemistry research to explore novel reactions and pathways, contributing to the advancement of synthetic methodologies. Its bromine moiety makes it a versatile building block for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,800.00 |
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| 1.000 | 10-20 days | ฿3,546.00 |
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| 5.000 | 10-20 days | ฿10,836.00 |
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| 10.000 | 10-20 days | ฿16,542.00 |
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2-Amino-8-bromo[1,2,4]triazolo[1,5-a]pyridine
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and psychiatric disorders. Its structural framework is often incorporated into compounds being studied for their potential as therapeutic agents, such as anxiolytics, anticonvulsants, or antipsychotics. Additionally, it is used in organic chemistry research to explore novel reactions and pathways, contributing to the advancement of synthetic methodologies. Its bromine moiety makes it a versatile building block for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for drug discovery.
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