Methyl 2-(bromomethyl)-4-nitrobenzoate
≥95%
- Product Code: 115934
CAS:
133446-99-8
Molecular Weight: | 274.07 g./mol | Molecular Formula: | C₉H₈BrNO₄ |
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EC Number: | MDL Number: | MFCD11505948 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
Used primarily in organic synthesis as a versatile intermediate for constructing complex molecules. It serves as a key building block in the preparation of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, while the nitro group can be reduced to an amine for additional modifications. It is also employed in the synthesis of agrochemicals and dyes, where its reactive sites enable the creation of diverse chemical structures. Additionally, it finds use in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
Product Specification:
Test | Specification |
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Appearance | White To Off-White Solid |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $79.84 |
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0.250 | 10-20 days | $139.48 |
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1.000 | 10-20 days | $309.49 |
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Methyl 2-(bromomethyl)-4-nitrobenzoate
Used primarily in organic synthesis as a versatile intermediate for constructing complex molecules. It serves as a key building block in the preparation of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs). The bromomethyl group allows for further functionalization through nucleophilic substitution reactions, while the nitro group can be reduced to an amine for additional modifications. It is also employed in the synthesis of agrochemicals and dyes, where its reactive sites enable the creation of diverse chemical structures. Additionally, it finds use in research laboratories for studying reaction mechanisms and developing new synthetic methodologies.
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