- 2-Nitrophenylacetonitrile
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- $100.00 / 1KG
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2023-12-26
- CAS:610-66-2
- Min. Order: 1KG
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 2-Nitrophenylacetonitrile Basic information |
| | 2-Nitrophenylacetonitrile Chemical Properties |
| Melting point | 82-85 °C(lit.) | | Boiling point | 178°C | | density | 1.3264 (rough estimate) | | refractive index | 1.5770 (estimate) | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform, Ethyl Acetate | | form | Powder | | color | Light brown to brownish-gray | | Water Solubility | <0.01 g/100 mL at 20 ºC | | BRN | 1869400 | | Exposure limits | NIOSH: IDLH 25 mg/m3 | | Stability: | Stable. Incompatible with strong oxidizing agents. | | CAS DataBase Reference | 610-66-2(CAS DataBase Reference) | | EPA Substance Registry System | o-Nitrophenylacetonitrile (610-66-2) |
| Hazard Codes | Xn,Xi | | Risk Statements | 20/21/22-36/37/38 | | Safety Statements | 26-36-24/25 | | RIDADR | 3439 | | WGK Germany | 3 | | RTECS | AM1248000 | | Hazard Note | Irritant | | TSCA | Yes | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 29269090 |
| | 2-Nitrophenylacetonitrile Usage And Synthesis |
| Chemical Properties | Yellow Solid | | Uses | 2-Nitrophenylacetonitrile was used in synthesis of 2 or 2,4-substituted α-carbolines via a one-pot tandem reaction of α,β-unsaturated ketones. It was used in the synthesis of strychnine. | | Synthesis Reference(s) | Synthesis, p. 514, 1987 DOI: 10.1055/s-1987-27989 | | General Description | Light brown solid. | | Air & Water Reactions | Insoluble in water. | | Reactivity Profile | Nitriles, such as 2-Nitrophenylacetonitrile, may polymerize in the presence of metals and some metal compounds. They are incompatible with acids; mixing nitriles with strong oxidizing acids can lead to extremely violent reactions. Nitriles are generally incompatible with other oxidizing agents such as peroxides and epoxides. The combination of bases and nitriles can produce hydrogen cyanide. Nitriles are hydrolyzed in both aqueous acid and base to give carboxylic acids (or salts of carboxylic acids). These reactions generate heat. Peroxides convert nitriles to amides. Nitriles can react vigorously with reducing agents. Acetonitrile and propionitrile are soluble in water, but nitriles higher than propionitrile have low aqueous solubility. They are also insoluble in aqueous acids. | | Fire Hazard | Flash point data for 2-Nitrophenylacetonitrile are not available. 2-Nitrophenylacetonitrile is probably combustible. |
| | 2-Nitrophenylacetonitrile Preparation Products And Raw materials |
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