Methyl 2-(bromomethyl)-3-methoxybenzoate
≥95%
- Product Code: 116811
CAS:
71887-28-0
| Molecular Weight: | 259.10 g./mol | Molecular Formula: | C₁₀H₁₁BrO₃ |
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| EC Number: | MDL Number: | MFCD04114320 | |
| Melting Point: | Boiling Point: | 330°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is widely used in organic synthesis as a versatile building block for the preparation of various pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its bromomethyl group makes it highly reactive, enabling it to participate in nucleophilic substitution reactions, which are essential for constructing carbon-carbon or carbon-heteroatom bonds. Additionally, the methoxy and ester functional groups provide further reactivity and selectivity, making it useful in multi-step synthetic routes. Its applications extend to the production of fine chemicals and specialty materials, where precise molecular modifications are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $44.01 |
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| 1.000 | 10-20 days | $87.76 |
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Methyl 2-(bromomethyl)-3-methoxybenzoate
This compound is widely used in organic synthesis as a versatile building block for the preparation of various pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). Its bromomethyl group makes it highly reactive, enabling it to participate in nucleophilic substitution reactions, which are essential for constructing carbon-carbon or carbon-heteroatom bonds. Additionally, the methoxy and ester functional groups provide further reactivity and selectivity, making it useful in multi-step synthetic routes. Its applications extend to the production of fine chemicals and specialty materials, where precise molecular modifications are required.
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