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| | 1-Phenyl-2-nitropropene Basic information |
| | 1-Phenyl-2-nitropropene Chemical Properties |
| Melting point | 63-65 °C (lit.) | | Boiling point | 263.0±9.0 °C(Predicted) | | density | 1.141±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | Acetone, Chloroform, Dichloromethane, Methanol | | form | Crystalline Powder | | color | Yellow | | InChI | InChI=1S/C9H9NO2/c1-8(10(11)12)7-9-5-3-2-4-6-9/h2-7H,1H3 | | InChIKey | WGSVFWFSJDAYBM-BQYQJAHWSA-N | | SMILES | C1(C=C([N+]([O-])=O)C)=CC=CC=C1 | | NIST Chemistry Reference | Benzene, (2-nitro-1-propenyl)-(705-60-2) | | EPA Substance Registry System | (2-Nitro-1-propenyl)benzene (705-60-2) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36-37/39 | | WGK Germany | 3 | | RTECS | DA6495000 | | HS Code | 29042090 |
| | 1-Phenyl-2-nitropropene Usage And Synthesis |
| Chemical Properties | Yellow crystalline powder | | Uses | 1-phenyl-2-nitropropene is used in the production of pharmaceuticals, for instance, for drug Adderall, a drug used to treat ADHD and narcolepsy. | | Application | (2-Nitropropenyl)benzene is a derivative of styrene (S687790), which exhibits herbicidal and antibacterial properties. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 15, p. 8, 1950 DOI: 10.1021/jo01147a002
Tetrahedron Letters, 26, p. 1193, 1985 DOI: 10.1016/S0040-4039(00)98431-4 | | General Description | trans-β-Methyl-β-nitrostyrene (1-phenyl-2-nitropropene), a nitrostyrene derivative is an α,β-disubstituted nitroalkene. It has been synthesized by reacting benzaldehyde with nitroethane and butylamine. Spectroscopic analysis of 1-phenyl-2-nitropropene has been done using FT-IR, FT-Raman, NMR and UV. |
| | 1-Phenyl-2-nitropropene Preparation Products And Raw materials |
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