36994-29-3

Basic information

• Product Name: 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one
• Synonyms: 3-(Dimethylamino)-1-(4-nitrophenyl)-1-propanone; 1-[3-(dimethylamino)-4-nitrophenyl]propan-1-one
• CAS NO: 36994-29-3
• Molecular Formula: C₁₁H₁₄N₂O₃*ClH
• Molecular Weight: 222.2405
• Mol File: 36994-29-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 364.4°C at 760 mmHg
• Flash Point: 174.2°C
• Density: 1.186g/cm³
• Vapor Pressure: 1.69E-05mmHg at 25°C
• Refractive Index: 1.573
• CAS DataBase Reference: 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one(36994-29-3)
• EPA Substance Registry System: 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one(36994-29-3)

Safety Data

• Hazardous Substances Data: 36994-29-3(Hazardous Substances Data)

Usage

General Description

3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one, also known as 4'-DMA-2'-oxo-PCE, is a synthetic chemical compound that belongs to the class of arylcyclohexylamines. It is a substituted derivative of phencyclidine (PCP) and acts as a dissociative anesthetic and hallucinogen. 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one has psychotropic effects and is known for its potential to induce hallucinations, euphoria, and sensory distortions. It has been identified as a designer drug and is illegal in many jurisdictions due to its potential for abuse and addiction. The safety and long-term health effects of 3-(dimethylamino)-1-(4-nitrophenyl)propan-1-one are not fully understood, and its use is associated with significant risks to physical and mental health.

Upstream product

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

Downstream Products

• 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 
• 91429-99-1 1-(4-amino-phenyl)-3-dimethylamino-propan-1-one 
• 100616-44-2 3-morpholin-4-yl-1-(4-nitro-phenyl)-propan-1-one 
• 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 
• 1072137-51-9 β-phenylamino-p-nitropropiophenone hydrochloride 
• 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 
• 88384-30-9 Carbonic acid 3-dimethylamino-1-(4-nitro-phenyl)-propyl ester phenyl ester; hydrochloride 
• 22731-72-2 1-(4-nitrophenyl)prop-2-en-1-one 
• 283610-70-8 2,3-dihydro-4-(4-nitrophenyl)-1H-1,5-benzodiazepine 

Relevant articles and documents

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.

Synthesis and pharmacologic assessment of carbamic and carbonic acid esters with 1-aryl-3-dimethylamino-1-propanols. III

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