3,5-Dibromo-1,2-phenylenediamine Monohydrochloride
98%
- Product Code: 44056
CAS:
75568-11-5
| Molecular Weight: | 302.39 g./mol | Molecular Formula: | C₆H₆Br₂N₂HCl |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012967 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Store at 2-8°C, filled with argon |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of dyes and pigments. Its structure allows for the creation of complex molecules, particularly in the development of colorants for textiles and plastics. Additionally, it is utilized in the synthesis of pharmaceuticals, where it acts as a building block for active pharmaceutical ingredients (APIs). Its bromine atoms make it valuable in cross-coupling reactions, which are essential in creating advanced materials and specialty chemicals. The compound is also employed in research settings for studying chemical reactions involving halogenated aromatic amines.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow red crystal powder |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,760.00 |
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| 0.500 | 10-20 days | ฿22,000.00 |
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| 1.000 | 10-20 days | ฿33,000.00 |
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3,5-Dibromo-1,2-phenylenediamine Monohydrochloride
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of dyes and pigments. Its structure allows for the creation of complex molecules, particularly in the development of colorants for textiles and plastics. Additionally, it is utilized in the synthesis of pharmaceuticals, where it acts as a building block for active pharmaceutical ingredients (APIs). Its bromine atoms make it valuable in cross-coupling reactions, which are essential in creating advanced materials and specialty chemicals. The compound is also employed in research settings for studying chemical reactions involving halogenated aromatic amines.
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