36994-29-3

Usage

Uses

Used in Research Applications:
3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one is utilized as a research chemical for studying the effects of dissociative anesthetics and hallucinogens on the human brain. Its use in scientific research aids in understanding the mechanisms of action and potential therapeutic applications of similar compounds.
Used in Forensic Analysis:
In the forensic science industry, 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one is used as a reference material for the detection and identification of designer drugs in criminal investigations. This helps law enforcement agencies to combat the distribution and abuse of illicit substances.

Upstream product

• 50-00-0 formaldehyd 
• 506-59-2 N,N-dimethylammonium chloride 
• 100-19-6 (4-nitrophenyl)ethanone 
• 110-88-3 1,3,5-Trioxan 

Downstream Products

• 100616-44-2 3-morpholin-4-yl-1-(4-nitro-phenyl)-propan-1-one 
• 140845-87-0 2-(4-Nitro-phenyl)-1,4-dihydro-benzo[4,5]imidazo[1,2-a]pyrimidine 
• 88384-27-4 3-dimethylamino-1-(4-nitro-phenyl)-propan-1-ol 
• 19832-76-9 3-anilino-1-(4-nitro-phenyl)-propan-1-one 
• 474975-42-3 7-hydroxy-2-methoxy-3-methyl-7-(4-nitrophenyl)-5,6,7,8-tetrahydropyrido[2,3-d]pyrimidin-4(3H)-one 
• 474975-41-2 6-amino-2-methoxy-3-methyl-5-[3-(4-nitrophenyl)-3-oxopropyl]pyrimidin-4(3H)-one 
• 1072137-51-9 β-phenylamino-p-nitropropiophenone hydrochloride 
• 107516-30-3 1-(4-nitro-phenyl)-3-piperidino-propan-1-one 
• 1607450-33-8 2-(benzylamino)-8,9-dihydro-6-(4-nitrophenyl)-3H-pyrimido[4,5-b][1,4]diazepin-4(7H)-one 
• 79045-77-5 2-Chloro-3-(4-methoxy-phenyl)-6-(4-nitro-phenyl)-3,4-dihydro-[1,3,2]oxazaphosphinine 2-oxide 
• 78993-98-3 2-Chloro-6-(4-nitro-phenyl)-3-p-tolyl-3,4-dihydro-[1,3,2]oxazaphosphinine 2-oxide 
• 78993-97-2 2-Chloro-6-(4-nitro-phenyl)-3-phenyl-3,4-dihydro-[1,3,2]oxazaphosphinine 2-oxide 
• 95886-38-7 2-Chloro-3-(3-methoxy-phenyl)-6-(4-nitro-phenyl)-3,4-dihydro-[1,3,2]oxazaphosphinine 2-oxide 

Relevant academic research and scientific papers

Selective hydrogenation of aromatic aminoketones by Pd/C catalysis

We report an alternative hydrogenation of aromatic aminoketones by heterogeneous catalyst of palladium on carbon (Pd/C) in which nitro, in particular carbonyl groups in the ketones, could be selectively transformed to corresponding amino ketone, secondary alcohol, or methylene compound. Copyright Taylor & Francis Group, LLC.

Dramatically accelerated synthesis of β-aminoketones via aqueous Mannich reaction under combined microwave and ultrasound irradiation

An efficient green chemistry approach to the synthesis of β-aminoketones was developed under combined microwave and ultrasound irradiation. With this technique, the title compounds were rapidly synthesized in aqueous media with good yields. Georg Thieme Verlag Stuttgart.