Methyl 4-bromo-3,5-dimethylbenzoate
97%
- Product Code: 47423
CAS:
432022-88-3
| Molecular Weight: | 243.10 g./mol | Molecular Formula: | C₁₀H₁₁BrO₂ |
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| EC Number: | MDL Number: | MFCD09833419 | |
| Melting Point: | Boiling Point: | 310.8°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
Methyl 4-bromo-3,5-dimethylbenzoate is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows it to serve as a building block for more complex molecules, often in the development of active pharmaceutical ingredients (APIs) or crop protection agents. The bromine atom in the compound makes it a valuable substrate for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are widely employed in drug discovery and material science. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its versatility in synthetic chemistry. The compound is also utilized in research settings for studying reaction mechanisms or developing new synthetic methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $18.09 |
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| 0.250 | 10-20 days | $29.97 |
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| 1.000 | 10-20 days | $87.76 |
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| 5.000 | 10-20 days | $272.46 |
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Methyl 4-bromo-3,5-dimethylbenzoate
Methyl 4-bromo-3,5-dimethylbenzoate is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows it to serve as a building block for more complex molecules, often in the development of active pharmaceutical ingredients (APIs) or crop protection agents. The bromine atom in the compound makes it a valuable substrate for further functionalization through cross-coupling reactions, such as Suzuki or Heck reactions, which are widely employed in drug discovery and material science. Additionally, its ester group can be hydrolyzed or transformed into other functional groups, enhancing its versatility in synthetic chemistry. The compound is also utilized in research settings for studying reaction mechanisms or developing new synthetic methodologies.
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