Methyl 2-(3-bromopyridin-4-yl)acetate
98%
- Product Code: 58594
CAS:
162615-12-5
| Molecular Weight: | 230.0586 g./mol | Molecular Formula: | C₈H₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10000071 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety, makes it valuable for constructing complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functional groups or build heterocyclic frameworks. Additionally, it serves as a precursor in the production of compounds with potential biological activities, including antimicrobial, antiviral, or anticancer properties. Its ester group also allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,000.00 |
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| 0.250 | 10-20 days | ฿15,300.00 |
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| 1.000 | 10-20 days | ฿38,700.00 |
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Methyl 2-(3-bromopyridin-4-yl)acetate
This chemical is primarily used in organic synthesis as a key intermediate for the development of various pharmaceuticals and agrochemicals. Its structure, featuring a bromopyridine moiety, makes it valuable for constructing complex molecules, particularly in the synthesis of active pharmaceutical ingredients (APIs). It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce functional groups or build heterocyclic frameworks. Additionally, it serves as a precursor in the production of compounds with potential biological activities, including antimicrobial, antiviral, or anticancer properties. Its ester group also allows for further chemical modifications, making it versatile in medicinal chemistry and drug discovery processes.
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