4-Bromo-2-ethylpyridine
98%
- Product Code: 119272
CAS:
156761-88-5
| Molecular Weight: | 186.05 g./mol | Molecular Formula: | C₇H₈BrN |
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| EC Number: | MDL Number: | MFCD11223216 | |
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| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
4-Bromo-2-ethylpyridine is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a building block for the development of more complex molecules, often contributing to the creation of active pharmaceutical ingredients (APIs) or crop protection agents. Its bromine atom makes it a valuable reagent for cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in constructing carbon-carbon bonds. Additionally, it can be utilized in the synthesis of ligands for catalysis or in the preparation of heterocyclic compounds with potential biological activity. Its applications are largely focused on research and development, where it aids in the discovery of new drugs or functional materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £82.03 |
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| 0.250 | 10-20 days | £143.30 |
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| 1.000 | 10-20 days | £358.05 |
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4-Bromo-2-ethylpyridine
4-Bromo-2-ethylpyridine is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a building block for the development of more complex molecules, often contributing to the creation of active pharmaceutical ingredients (APIs) or crop protection agents. Its bromine atom makes it a valuable reagent for cross-coupling reactions, such as Suzuki or Heck reactions, which are essential in constructing carbon-carbon bonds. Additionally, it can be utilized in the synthesis of ligands for catalysis or in the preparation of heterocyclic compounds with potential biological activity. Its applications are largely focused on research and development, where it aids in the discovery of new drugs or functional materials.
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