5-Bromo-2-(bromomethyl)pyridine hydrobromide
97%
- Product Code: 48894
CAS:
173999-22-9
| Molecular Weight: | 331.83 g./mol | Molecular Formula: | C₆H₆Br₃N |
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| EC Number: | MDL Number: | MFCD20921831 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target neurological and inflammatory disorders. Its bromomethyl group makes it a valuable reagent for introducing functional groups or creating complex molecular structures through nucleophilic substitution reactions. Additionally, it is employed in the research and development of agrochemicals, where it contributes to the creation of novel pesticides and herbicides. Its role in medicinal chemistry also extends to the design of potential drug candidates for treating infectious diseases, leveraging its pyridine core for enhanced biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft49,065.29 |
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| 1.000 | 10-20 days | Ft98,130.58 |
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| 5.000 | 10-20 days | Ft232,720.73 |
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5-Bromo-2-(bromomethyl)pyridine hydrobromide
This chemical is primarily utilized in organic synthesis as a versatile building block for the preparation of various heterocyclic compounds. It serves as a key intermediate in the development of pharmaceuticals, particularly in the synthesis of active pharmaceutical ingredients (APIs) that target neurological and inflammatory disorders. Its bromomethyl group makes it a valuable reagent for introducing functional groups or creating complex molecular structures through nucleophilic substitution reactions. Additionally, it is employed in the research and development of agrochemicals, where it contributes to the creation of novel pesticides and herbicides. Its role in medicinal chemistry also extends to the design of potential drug candidates for treating infectious diseases, leveraging its pyridine core for enhanced biological activity.
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