Methyl 2-amino-3-bromobenzoate
97%
- Product Code: 104558
CAS:
104670-74-8
| Molecular Weight: | 230.07 g./mol | Molecular Formula: | C₈H₈BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11042862 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring both an amino group and a bromine atom, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are crucial in drug development. Its ester group also allows for further functionalization, enabling the creation of a wide range of derivatives for research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity (%) | 96.5-100 |
| Melting Point | 45 Degree Celsius-49 Degree Celsius |
| Appearance | Solid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿342.00 |
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| 5.000 | 10-20 days | ฿1,071.00 |
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| 25.000 | 10-20 days | ฿5,337.00 |
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Methyl 2-amino-3-bromobenzoate
This compound is primarily utilized in organic synthesis, particularly as an intermediate in the production of pharmaceuticals and agrochemicals. Its structure, featuring both an amino group and a bromine atom, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create biologically active compounds. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are crucial in drug development. Its ester group also allows for further functionalization, enabling the creation of a wide range of derivatives for research and industrial applications.
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