N,N-Dimethyl 4-bromo-3-nitrobenzylamine
97%
- Product Code: 121302
CAS:
1414029-51-8
| Molecular Weight: | 259.10 g./mol | Molecular Formula: | C₉H₁₁BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22574936 | |
| Melting Point: | Boiling Point: | 289.0±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
N,N-Dimethyl 4-bromo-3-nitrobenzylamine is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a bromo and nitro group, makes it suitable for various substitution and coupling reactions, which are fundamental in the development of pharmaceuticals and agrochemicals. The compound is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the nitro group can be reduced to an amine, and the bromo group can undergo further functionalization, such as in palladium-catalyzed cross-coupling reactions. Additionally, it serves as a building block in the creation of dyes, pigments, and other specialty chemicals, where its aromatic core and reactive sites allow for tailored modifications to achieve desired properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿945.00 |
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| 0.250 | 10-20 days | ฿1,872.00 |
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N,N-Dimethyl 4-bromo-3-nitrobenzylamine
N,N-Dimethyl 4-bromo-3-nitrobenzylamine is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex chemical compounds. Its structure, featuring both a bromo and nitro group, makes it suitable for various substitution and coupling reactions, which are fundamental in the development of pharmaceuticals and agrochemicals. The compound is often employed in the synthesis of active pharmaceutical ingredients (APIs) where the nitro group can be reduced to an amine, and the bromo group can undergo further functionalization, such as in palladium-catalyzed cross-coupling reactions. Additionally, it serves as a building block in the creation of dyes, pigments, and other specialty chemicals, where its aromatic core and reactive sites allow for tailored modifications to achieve desired properties.
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