Methyl 4-bromo-3-methylbenzoate
99%
- Product Code: 205419
CAS:
148547-19-7
| Molecular Weight: | 229.07 g./mol | Molecular Formula: | C₉H₉BrO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00673014 | |
| Melting Point: | 38-44 °C(lit.) | Boiling Point: | |
| Density: | 1.433 g/cm3 | Storage Condition: | Room temperature, sealed |
Product Description:
Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block for the preparation of more complex molecules, including active pharmaceutical ingredients (APIs), due to the presence of both bromo and ester functional groups, which allow for further transformations such as cross-coupling reactions. The compound is also employed in the development of novel compounds in medicinal chemistry research, where the aromatic scaffold with specific substitution patterns is required. Its methyl ester group can be hydrolyzed to yield the corresponding carboxylic acid, enabling conjugation or further derivatization. Additionally, it finds use in the synthesis of functional materials and specialty chemicals where substituted aromatic esters are needed.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | ฿144.00 |
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| 5g | 10-20 days | ฿390.00 |
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| 25g | 10-20 days | ฿1,400.00 |
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| 100g | 10-20 days | ฿5,560.00 |
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Methyl 4-bromo-3-methylbenzoate
Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. It serves as a building block for the preparation of more complex molecules, including active pharmaceutical ingredients (APIs), due to the presence of both bromo and ester functional groups, which allow for further transformations such as cross-coupling reactions. The compound is also employed in the development of novel compounds in medicinal chemistry research, where the aromatic scaffold with specific substitution patterns is required. Its methyl ester group can be hydrolyzed to yield the corresponding carboxylic acid, enabling conjugation or further derivatization. Additionally, it finds use in the synthesis of functional materials and specialty chemicals where substituted aromatic esters are needed.
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