4-Bromo-2-methyl-6-nitroaniline
98%
- Product Code: 72391
Alias:
4-Bromo-6-nitro-o-toluidine
2-amino-5-bromo-3-nitrotoluene
CAS:
77811-44-0
| Molecular Weight: | 231.05 g./mol | Molecular Formula: | H₃CC₆H₂BrNO₂NH₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00052919 | |
| Melting Point: | 143-147 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely applied in textiles, leather, and paper industries. It also finds application in the development of organic compounds for research purposes, especially in studies involving nitroaniline derivatives. Additionally, it may be utilized in the preparation of pharmaceutical intermediates, contributing to the synthesis of various active pharmaceutical ingredients. Its role in chemical synthesis is significant due to its reactive functional groups, enabling diverse transformations in organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 144-148 |
| PurityGC | 98-100 |
| APPEARANCE | WHITE TO YELLOW TO BROWN POWDER AND/OR CHUNKS |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿280.00 |
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| 5.000 | 10-20 days | ฿680.00 |
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| 25.000 | 10-20 days | ฿2,020.00 |
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| 100.000 | 10-20 days | ฿6,820.00 |
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4-Bromo-2-methyl-6-nitroaniline
Used primarily as an intermediate in the synthesis of dyes and pigments, particularly in the production of azo dyes, which are widely applied in textiles, leather, and paper industries. It also finds application in the development of organic compounds for research purposes, especially in studies involving nitroaniline derivatives. Additionally, it may be utilized in the preparation of pharmaceutical intermediates, contributing to the synthesis of various active pharmaceutical ingredients. Its role in chemical synthesis is significant due to its reactive functional groups, enabling diverse transformations in organic chemistry.
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