4-Nitrobenzenediazonium Tetrafluoroborate
97%
- Product Code: 91152
CAS:
456-27-9
| Molecular Weight: | 236.92 g./mol | Molecular Formula: | C₆H₄BF₄N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00012005 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, inert gas storage |
Product Description:
This chemical is primarily used in organic synthesis as a diazonium salt, which is highly reactive and serves as a key intermediate in various chemical reactions. It is commonly employed in the preparation of azo dyes, where it acts as a coupling agent to produce vibrant and stable colorants for textiles, inks, and pigments. Additionally, it is utilized in the synthesis of aryl compounds through Sandmeyer reactions, enabling the introduction of nitro groups into aromatic systems. Its role in photoaffinity labeling is also notable, as it helps in studying molecular interactions and binding sites in biochemical research. Due to its reactivity, it is often handled with care in controlled environments.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale yellow to brown solid |
| PURITY | 96.5 |
| MELTING POINT | 140-150 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,180.00 |
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| 5.000 | 10-20 days | ฿4,390.00 |
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| 25.000 | 10-20 days | ฿11,680.00 |
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| 100.000 | 10-20 days | ฿45,500.00 |
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4-Nitrobenzenediazonium Tetrafluoroborate
This chemical is primarily used in organic synthesis as a diazonium salt, which is highly reactive and serves as a key intermediate in various chemical reactions. It is commonly employed in the preparation of azo dyes, where it acts as a coupling agent to produce vibrant and stable colorants for textiles, inks, and pigments. Additionally, it is utilized in the synthesis of aryl compounds through Sandmeyer reactions, enabling the introduction of nitro groups into aromatic systems. Its role in photoaffinity labeling is also notable, as it helps in studying molecular interactions and binding sites in biochemical research. Due to its reactivity, it is often handled with care in controlled environments.
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