Methyl 3-bromobenzoate
98%
- Product Code: 78239
CAS:
618-89-3
Molecular Weight: | 215.0400 g./mol | Molecular Formula: | C₈H₇BrO₂ |
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EC Number: | MDL Number: | MFCD00017777 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Methyl 3-bromobenzoate is widely used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block in the development of complex molecules, enabling the introduction of the bromo and ester functional groups into target compounds. In pharmaceutical research, it is utilized in the synthesis of active pharmaceutical ingredients (APIs) and drug candidates, often playing a role in the creation of anti-inflammatory, antimicrobial, and anticancer agents. Additionally, it finds application in material science, where it contributes to the development of specialty chemicals and polymers. Its reactivity makes it valuable in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in organic chemistry.
Product Specification:
Test | Specification |
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PURITYHPLC | 97.5 100% |
Appearance | white-yellow powder |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿360.00 |
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25.000 | 10-20 days | ฿1,190.00 |
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100.000 | 10-20 days | ฿4,620.00 |
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Methyl 3-bromobenzoate
Methyl 3-bromobenzoate is widely used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. It serves as a key building block in the development of complex molecules, enabling the introduction of the bromo and ester functional groups into target compounds. In pharmaceutical research, it is utilized in the synthesis of active pharmaceutical ingredients (APIs) and drug candidates, often playing a role in the creation of anti-inflammatory, antimicrobial, and anticancer agents. Additionally, it finds application in material science, where it contributes to the development of specialty chemicals and polymers. Its reactivity makes it valuable in cross-coupling reactions, such as Suzuki and Heck reactions, which are essential for constructing carbon-carbon bonds in organic chemistry.
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