16735-30-1

Basic information

• Product Name: 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE
• Synonyms: 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE
• CAS NO: 16735-30-1
• Molecular Formula: C₁₇H₁₉NO
• Molecular Weight: 253.33886
• Mol File: 16735-30-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE(16735-30-1)
• EPA Substance Registry System: 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE(16735-30-1)

Safety Data

• Hazardous Substances Data: 16735-30-1(Hazardous Substances Data)

Usage

General Description

2-(Benzyl methyl amino)-1-phenylpropan-1-one is a chemical compound with the molecular formula C17H19NO. It is a synthetic organic compound that belongs to the ketone class of chemicals. 2-(BENZYL METHYL AMINO)-1-PHENYLPROPAN-1-ONE is often used in research and scientific experiments, and may also have applications in the pharmaceutical and medical industries. It is important to handle this chemical with care, as it can be hazardous if not used properly and should only be handled by qualified individuals with proper safety equipment and procedures.

Upstream product

• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 103-67-3 benzyl-methyl-amine 
• 37471-46-8 1-phenyl-1-trimethylsiloxypropene 
• 93-55-0 1-phenyl-propan-1-one 
• 6084-17-9 2-chloro-1-phenylpropan-1-one 

Downstream Products

• 299-42-3 ephedrine 
• 90-82-4 pseudoephedrine 
• 159099-80-6 (1S,2S)-2-(N-benzyl-N-methylamino)-1-phenyl-1-propanol 
• 5650-44-2 methcathinone 
• 90-85-7 (1RS,2RS)-2-(benzyl-methyl-amino)-1-phenyl-propan-1-ol 
• 90-81-3 ephedrine 
• 73081-72-8 1,3,5-trimethyl-4-phenyl-1,5-dihydro-2-pyrrolone 
• 877869-98-2 3-butyl-1,5-dimethyl-4-phenyl-1,5-dihydro-2-pyrrolone 
• 877869-97-1 3-isopropyl-1,5-dimethyl-4-phenyl-1,5-dihydro-2-pyrrolone 
• 160977-88-8 (+)-Methcathinone 
• 5650-44-2 (-)-Methcathinone 
• 52340-16-6 (1R,2S)-1-cyclohexyl-2-methylamino-propan-1-ol 
• 537-46-2 Methamphetamin 
• 60065-37-4 (+)(2Ξ,3S)-3-methylamino-2-phenyl-butan-2-ol 

Relevant articles and documents

Electrochemically Oxidative α-C-H Functionalization of Ketones: A Cascade Synthesis of α-Amino Ketones Mediated by NH4I

An efficient electrochemical protocol for the synthesis of α-amino ketones via the oxidative cross-dehydrogenative coupling of ketones and secondary amines has been developed. The electrochemistry performs in a simple undivided cell using NH4I

Transition-metal-free oxidative α-C-H amination of ketones via a radical mechanism: Mild synthesis of α-amino ketones

A transition-metal-free direct α-C.H amination of ketones has been developed using commercially available ammonium iodide as the catalyst and sodium percarbonate as the co-oxidant. A wide range of ketone ((hetero)aromatic or nonaromatic ketones) and amine (primary/secondary amines, anilines, or amides) substrates undergo cross-coupling to generate synthetically useful α-amino ketones. The mechanistic studies indicated that a radical pathway might be involved in the reaction process. The utility of the method is highlighted through a concise one-step synthesis of the pharmaceutical agent amfepramone.