2-Bromo-3,5-dinitrobenzoic acid
98%
- Product Code: 43166
CAS:
116529-60-3
| Molecular Weight: | 291.01 g./mol | Molecular Formula: | C₇H₃BrN₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00458630 | |
| Melting Point: | Boiling Point: | 382.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
2-Bromo-3,5-dinitrobenzoic acid is primarily used in organic synthesis as a reagent or intermediate. Its structure, featuring both nitro and bromo groups, makes it valuable for introducing functional groups into aromatic compounds. It is often employed in the preparation of more complex molecules, particularly in pharmaceutical research, where it can be used to develop active pharmaceutical ingredients (APIs). Additionally, it serves as a building block in the synthesis of dyes, pigments, and other specialty chemicals. Its reactivity also makes it useful in studies involving electrophilic aromatic substitution reactions, aiding in the exploration of reaction mechanisms and the development of new synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Yellow Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿380.00 |
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| 1.000 | 10-20 days | ฿940.00 |
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| 5.000 | 10-20 days | ฿2,980.00 |
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| 10.000 | 10-20 days | ฿5,360.00 |
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| 25.000 | 10-20 days | ฿9,980.00 |
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2-Bromo-3,5-dinitrobenzoic acid
2-Bromo-3,5-dinitrobenzoic acid is primarily used in organic synthesis as a reagent or intermediate. Its structure, featuring both nitro and bromo groups, makes it valuable for introducing functional groups into aromatic compounds. It is often employed in the preparation of more complex molecules, particularly in pharmaceutical research, where it can be used to develop active pharmaceutical ingredients (APIs). Additionally, it serves as a building block in the synthesis of dyes, pigments, and other specialty chemicals. Its reactivity also makes it useful in studies involving electrophilic aromatic substitution reactions, aiding in the exploration of reaction mechanisms and the development of new synthetic pathways.
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