69957-35-3

Usage

Uses

Used in Pharmaceutical Industry:
(2-nitro-3-phenyl-propyl)benzene is used as an intermediate in the synthesis of various pharmaceutical compounds for its versatile chemical structure and reactivity.
Used in Chemical Industry:
(2-nitro-3-phenyl-propyl)benzene is used as a building block in the production of dyes, fragrances, and other specialty chemicals due to its unique properties and functional groups.
Used in Organic Synthesis:
(2-nitro-3-phenyl-propyl)benzene is used as a key component in the synthesis of various organic compounds, taking advantage of its reactive nitro group and aromatic ring for further chemical transformations.

Upstream product

• 58497-32-8 (2-nitroprop-1-ene-1,3-diyl)dibenzene 
• 6125-24-2 2-Phenylnitroethane 
• 100-52-7 benzaldehyde 

Downstream Products

• 114090-62-9 methyl 4-benzyl-3-methyl-4-nitro-5-phenylpentanoate 
• 114090-88-9 trans-5,5-dibenzyl-1-hydroxy-4-methyl-3-phenylthiopyrrolidin-2-one 
• 114090-88-9 cis-5,5-dibenzyl-1-hydroxy-4-methyl-3-phenylthiopyrrolidin-2-one 
• 114090-52-7 (E)-4-benzyl-4-nitro-5-phenylpent-2-enal ethylene acetal 
• 89188-71-6 (Z)-4-benzyl-4-nitro-5-phenylpent-2-enal ethylene acetal 
• 114090-86-7 trans-5,5-dibenzyl-1-hydroxy-3-hydroxymethyl-4-methylpyrrolidin-2-one 
• 114090-86-7 cis-5,5-dibenzyl-1-hydroxy-3-hydroxymethyl-4-methylpyrrolidin-2-one 
• 114090-50-5 (E)-4-benzyl-4-nitro-5-phenylpent-2-en-1-ol 
• 114090-84-5 trans-5,5-dibenzyl-1-hydroxy-3,4-dimethylpyrrolidin-2-one 
• 114090-84-5 cis-5,5-dibenzyl-1-hydroxy-3,4-dimethylpyrrolidin-2-one 
• 114090-51-6 (E)-4-benzyl-4-nitro-5-phenylpent-2-enal 
• 114090-82-3 1-benzoyloxy-5,5-dibenzyl-4-methylpyrrolidin-2-one 
• 89188-72-7 (Z)-4-amino-4-benzyl-4-nitro-5-phenylpent-2-enal ethylene acetal 
• 114090-79-8 1-acetyl-5,5-dibenzyl-4-methylpyrrolidin-2-one 

Relevant academic research and scientific papers

Biosynthesis of Porphyrins and Related Macrocycles. Part 29. Synthesis and Chemistry of 2,2-Disubstituted 2H-Pyrroles (Pyrrolenines)

Syntheses are described of three 2H-pyrroles (pyrrolenines), (15), (28), and (64), which were designed to test the chemical feasibility of the rearrangements proposed as part of the mechanism of the enzyme cosynthetase (uroporphynogen III synthase).All three syntheses create the 2H-pyrrole ring by the Michael addition of nitronate anion to an α,β-unsaturated ester and one introduces an additional substituent by novel alkylations of the dianion of a hydroxamic acid.Some of intermediates in the syntheses showed unusual n.m.r. properties which reveal strong conformational preferences.The rearrangement of the 2H-pyrroles was studied under both thermal and acid-catalysed conditions.The results show that 2,2-disubstituted 2H-pyrroles only rearrange easily by -sigmatropic shifts if they do not have further substituents on C-3 and C-4. 2-Pyrrolylmethyl-2H-pyrroles prefer to rearrange by a fragmentation-recombination mechanism.