Methyl 2-(2-bromo-5-chlorophenyl)acetate
97%
- Product Code: 41382
CAS:
455957-76-3
| Molecular Weight: | 263.5156 g./mol | Molecular Formula: | C₉H₈BrClO₂ |
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| EC Number: | MDL Number: | MFCD18398721 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a valuable building block for constructing complex molecules. It is often employed in coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic functionalities into target compounds. Additionally, it serves as a precursor in the synthesis of active pharmaceutical ingredients (APIs) for drugs targeting neurological or inflammatory conditions. In agrochemical research, it is used to develop herbicides and pesticides due to its ability to modify biological activity in target organisms. Its ester group also allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £11.20 |
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Methyl 2-(2-bromo-5-chlorophenyl)acetate
This chemical is primarily utilized in organic synthesis as an intermediate for the production of various pharmaceuticals and agrochemicals. Its structure, featuring both bromo and chloro substituents, makes it a valuable building block for constructing complex molecules. It is often employed in coupling reactions, such as Suzuki or Heck reactions, to introduce aromatic functionalities into target compounds. Additionally, it serves as a precursor in the synthesis of active pharmaceutical ingredients (APIs) for drugs targeting neurological or inflammatory conditions. In agrochemical research, it is used to develop herbicides and pesticides due to its ability to modify biological activity in target organisms. Its ester group also allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.
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