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1-Phenyl-2-Nitropropene (P2NP) is an agent of greasy fragrant unsaturated nitro mixes. Remotely, it is a yellow needle-molded precious stones with an unconventional smell. It disturbs the mucous layers, leaves hard to-recuperate ulcers on the skin. Phenylnitropropene is profoundly CH-acidic.

IUPAC name: 1-Phenyl-2-nitropropene, 1-Phenyl-2-nitropropene

Regular names: 1 Phenyl 2 Nitropropene, 1-Phenyl-2-nitropropene, P2NP, P2NP, Phenylnitropropene, (2-nitropropen-1-yl), (2-Nitropropenyl) benzene, Phenyl-2-nitropropene, Wikipedol, nikropropene, Phenyl-2-nitropropene, Phenyl-2-nitropropene, Phenyl-2-nitropropene, (2-Nitropropenyl) benzene, Phenyl-2-nitropropene


Atomic equation: C9H9NO2

Molar mass: 163.17 g mol-1

Appearance: yellow needles

Liquefying point: 64-66 ° C

Dissolvability: insoluble in water, solvent in natural solvents (ethanol, cold acidic corrosive, acetonitrile, isopropanol, tetrahydrofuran (THF), diethyl ether)


1-Phenyl-2-nitropropene (phenyl-2-nitropropene, phenylnitropropene) has discovered application in fine natural amalgamation, specifically the blend of phenyl-2-propanol, phenyl-2-propanol oxime, phenyl-2-nitropropane, and others. Can likewise be utilized in the production of pharmaceuticals.

Nitropropene (synthetic reference)

Fairly later, by the progression hydrogenation of furylnitroethylene was diminished to 1-furyl-2-aminoethane. As indicated by patent information, 1-phenyl-2-nitropropen-1 by treatment with sodium amalgam in a liquor acidic corrosive medium was quickly changed over into 1-phenyl-2-aminopropane, disengaged as a salt.

The expansion of acetylene to nitromethane prompts 1-nitropropene. For this situation, the essential buildup item is viewed as 3-nitropropene, which at that point experiences a revision, moving the twofold cling to a place that guarantees its conjugation with the nitro gathering.

Nitro-olefins, thusly, can experience different changes, for instance, they can be decreased to the relating 1-phenyl-2-nitropropen-1 amines by hydrogenation within the sight of a Raney nickel impetus, yielding the comparing amine in 40% yield [61] From y-nitrostyrene by hydrogenation within the sight of platinum oxide, p-phenethylamine can be acquired in 93% yield, and 3,4-methylenedioxy-nitrostyrene and 3-nitrosy nitrostyrene within the sight of a similar impetus are hydrogenated to the relating amine 17.

Nitropropene (equation)


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