21970-65-0

Basic information

• Product Name: 3-[benzyl(methyl)amino]-1-phenylpropan-1-one
• Synonyms: 1-propanone, 3-[methyl(phenylmethyl)amino]-1-phenyl-; 3-[Benzyl(methyl)amino]-1-phenylpropan-1-one
• CAS NO: 21970-65-0
• Molecular Formula: C₁₇H₁₉NO
• Molecular Weight: 253.3389
• EINECS: 606-868-2
• Mol File: 21970-65-0.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 374.2°C at 760 mmHg
• Flash Point: 134.1°C
• Density: 1.062g/cm³
• Vapor Pressure: 8.5E-06mmHg at 25°C
• Refractive Index: 1.571
• Storage Temp.: Refrigerator, Under inert atmosphere
• Solubility: Chloroform (Slightly), DMSO (Slightly)
• CAS DataBase Reference: 3-[benzyl(methyl)amino]-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-[benzyl(methyl)amino]-1-phenylpropan-1-one(21970-65-0)
• EPA Substance Registry System: 3-[benzyl(methyl)amino]-1-phenylpropan-1-one(21970-65-0)

Safety Data

• Hazardous Substances Data: 21970-65-0(Hazardous Substances Data)

Usage

Uses

β-N-Benzyl-N''-methylaminopropiophenone is a useful reagent in asymmetric hydrogenation of amino ketones.

Upstream product

• 18636-32-3 3-methyllumiflavin 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 
• 100-52-7 benzaldehyde 
• 3623-15-2 phenyl propargyl ketone 
• 103-67-3 benzyl-methyl-amine 
• 936-59-4 3-chloropropiophenone 
• 6919-61-5 N-methoxy-N-methylbenzamide 
• 1826-67-1 vinyl magnesium bromide 
• 50-00-0 formaldehyd 
• 98-86-2 acetophenone 
• 93-55-0 1-phenyl-propan-1-one 
• 879-72-1 3-(dimethylamino)propiophenone hydrochloride 
• 13426-94-3 N-methylbenzylamine hydrochloride 

Downstream Products

• 651321-23-2 5-(benzyl-methyl-amino)-2,2-difluoro-3-hydroxy-3-phenylpentanoic acid ethyl ester 
• 873436-52-3 (S)-3-(benzyl(methyl)amino)-1-phenylpropan-1-ol 
• 21912-89-0 3-methylamino-1,1-diphenyl-propan-1-ol 
• 58215-93-3 3-methyl-6,6-diphenyl-tetrahydro-[1,3]oxazine 
• 651321-24-3 3,3-difluoro-4-hydroxy-1-methyl-4-phenylpiperidin-2-one 
• 159216-80-5 N-benzyl-N-methyl-3-(p-trifluoromethylphenoxy)-3-phenylpropyl-amine 
• 54910-89-3 FLUOXETINE 
• 74681-55-3 3-(N-benzyl-N-methylamino)-1-phenyl-propan-1-ol 
• 42142-52-9 3-methylamino-1-phenylpropan-1-ol 
• 27152-62-1 3-(N-methylamino)propiophenone 
• 25772-95-6 3-(benzyl-methyl-amino)-1,1-diphenyl-propan-1-ol 

Relevant articles and documents

Novel carbon-carbon bond formation between N-methyl-3-phenyl-3- hydroxypropylamine and cresols catalyzed by p-toluenesulphonic acid

The p-toluenesulphonic acid-catalyzed reaction between appropriate cresols and N-methyl-3-phenyl-3-hydroxypropylamine in refluxing toluene resulted in the formation of o -substituted phenol derivatives by an aromatic nucleophilic substitution reaction. Copyright Taylor & Francis Group, LLC.

PEG 400/cerium ammonium nitrate combined with microwave-assisted synthesis for rapid access to beta-amino ketones. an easy-to-use protocol for discovering new hit compounds

Compound libraries are important requirement in target-based drug discovery. In the present work, a small focused compound library based on β-aminoketone scaffold has been prepared combining microwave-assisted organic synthesis (MAOS) with polymer-assiste

Synthesis and antimicrobial activity of some new 1,2,4-triazine and benzimidazole derivatives

1-(4-Substituted phenyl)-3-(substituted)propan-1-(1H-benzo[d]imidazol-2-yl) hydrazines and 1-(4-substituted phenyl)- 3-(substituted)propan-1-(5H-[1,2,4] triazino[5,6-b]indol-3-yl) hydrazines have been synthesized by the fusion of triazine and benzimidazole derivatives with Mannich bases. The synthesized compounds have been characterized and screened against ITCC 5226 Sclerotium rolfsii and ITCC 0482 Macrophomina phaseolina and MTCC739 Escherichia coli, ATCC6533 Bacillus subtilis, ATCC9144 Staphylococcus aureus, ATCC25619 Pseudomonas aeruginosa and ATCC24433 Candida albicans.