Methyl 2-amino-4-bromo-5-methoxybenzoate
97%
- Product Code: 61794
CAS:
1256955-36-8
| Molecular Weight: | 260.09 g./mol | Molecular Formula: | C₉H₁₀BrNO₃ |
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| EC Number: | MDL Number: | MFCD28400710 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. Its structure, featuring both amino and bromo groups, makes it a versatile building block for further chemical modifications, such as coupling reactions or functional group transformations. Additionally, it can be used in research settings to study reaction mechanisms or to develop novel chemical entities with specific biological activities. Its methoxy and ester groups also contribute to its reactivity, enabling its use in the creation of fine chemicals and agrochemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $124.94 |
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| 0.250 | 10-20 days | $219.44 |
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| 1.000 | 10-20 days | $288.10 |
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Methyl 2-amino-4-bromo-5-methoxybenzoate
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of compounds with potential therapeutic properties. Its structure, featuring both amino and bromo groups, makes it a versatile building block for further chemical modifications, such as coupling reactions or functional group transformations. Additionally, it can be used in research settings to study reaction mechanisms or to develop novel chemical entities with specific biological activities. Its methoxy and ester groups also contribute to its reactivity, enabling its use in the creation of fine chemicals and agrochemicals.
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