Buy 1-Phenyl-2-Nitropropene (P2NP) Online | Order 1-Phenyl-2-Nitropropene (P2NP) Online

Buy 1-Phenyl-2-Nitropropene (P2NP) Online | Order 1-Phenyl-2-Nitropropene (P2NP) Online

Description

Buy 1-phenyl-2-nitropropene/P2NP online
Buy 1-phenyl-2-nitropropene (P2NP) online. 1-Phenyl-2-nitropropene (P2NP) is a representative of fatty aromatic nitro unsaturated compounds. Externally, it is a needle-shaped yellow crystal with a peculiar smell. It irritates the mucous membranes and leaves ulcers on the skin that are difficult to heal. Phenylnitropropene is highly acidic CH.

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

Common Names: 1 Phenyl 2 Nitropropene, 1-Phenyl-2-nitropropene, P2NP, P2NP, Phenylnitropropene, (2-nitropropen-1-yl), (2-Nitropropenyl)benzene, Phenyl-2-nitropropene, Wikipediadol, nikropropen, Phenyl -2-nitropropene, phenyl-2-nitropropene, phenyl-2-nitropropene, (2-nitropropenyl) benzene, phenyl-2-nitropropene

Properties:
Molecular formula: C9H9NO2
Molar mass: 163.17 g mol-1
Appearance: yellow needles
Melting point: 64-66°C

Solubility: insoluble in water, soluble in organic solvents (ethanol, glacial acetic acid, acetonitrile, isopropanol, tetrahydrofuran (THF), diethyl ether)

Application:
1-phenyl-2-nitropropene (phenyl-2-nitropropene, phenylnitropropene) has found application in fine organic synthesis, in particular the synthesis of phenyl-2-propanol, phenyl-2-propanol oxime, phenyl-2-nitropropane and others. Can also be used in the manufacture of pharmaceutical products.

Nitropropene (chemical reference)
A little later, through the hydrogenation step furylnitroethylene was reduced to 1-furyl-2-aminoethane. According to patent data, 1-phenyl-2-nitropropene-1 by treatment with sodium amalgam in alcohol-acetic acid medium was immediately converted to 1-phenyl-2-aminopropane, isolated in salt form.

The addition of acetylene to nitromethane leads to 1-nitropropene. In this case, the primary condensation product is considered to be 3-nitropropene, which then undergoes a rearrangement, moving the double bond to a position that ensures its conjugation with the nitro group.

Nitro-olefins, in turn, can undergo various transformations, for example, they can be reduced to the corresponding 1-phenyl-2-nitropropen-1 amines by hydrogenation in the presence of a Raney nickel catalyst, giving the amine corresponding to 40%. yield [61] From y-nitrostyrene by hydrogenation in the presence of platinum oxide, p-phenethylamine can be obtained with a yield of 93% and 3,4-methylenedioxy-nitrostyrene and 3-nitrosy nitrostyrene in the presence of the same catalyst are hydrogenated to the corresponding amine 17.

Nitropropene (formula)
C9H9NO2