1-ANTHROYL CYANIDE
95%(HPLC)
- Product Code: 39682
Alias:
1-Anthracene cyanate; 1-diazonitrile; Anthracene-1-carbonyl cyanide; 1-AN, can be used for derivatization of T-2 toxin
CAS:
85985-43-9
| Molecular Weight: | 231.25 g./mol | Molecular Formula: | C₁₆H₉NO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 163～166℃ | Boiling Point: | 426.8±14.0°C |
| Density: | 1.266±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
1-Anthroyl cyanide is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex organic compounds, particularly in the synthesis of heterocyclic molecules. Its structure, featuring both an anthroyl group and a nitrile functional group, makes it valuable for constructing frameworks in pharmaceuticals and agrochemicals. Additionally, it serves as a key reagent in the development of fluorescent dyes and pigments due to its ability to absorb and emit light efficiently. In research, it is used to study reaction mechanisms and to develop new synthetic methodologies, particularly in the field of photochemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Orange crystal |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | Ft157,301.98 |
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| 0.005 | 10-20 days | Ft523,621.65 |
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1-ANTHROYL CYANIDE
1-Anthroyl cyanide is primarily utilized in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex organic compounds, particularly in the synthesis of heterocyclic molecules. Its structure, featuring both an anthroyl group and a nitrile functional group, makes it valuable for constructing frameworks in pharmaceuticals and agrochemicals. Additionally, it serves as a key reagent in the development of fluorescent dyes and pigments due to its ability to absorb and emit light efficiently. In research, it is used to study reaction mechanisms and to develop new synthetic methodologies, particularly in the field of photochemistry.
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