49681-82-5

Basic information

• Product Name: N,N-dimethyl-2-phenylpropan-1-amine
• CAS NO: 49681-82-5
• Molecular Formula: C₁₁H₁₇N
• Molecular Weight: 163.2594
• Mol File: 49681-82-5.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 216.5°C at 760 mmHg
• Flash Point: 76.8°C
• Density: 0.908g/cm³
• Vapor Pressure: 0.139mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: N,N-dimethyl-2-phenylpropan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dimethyl-2-phenylpropan-1-amine(49681-82-5)
• EPA Substance Registry System: N,N-dimethyl-2-phenylpropan-1-amine(49681-82-5)

Safety Data

• Hazardous Substances Data: 49681-82-5(Hazardous Substances Data)

Upstream product

• 14352-87-5 (+/-)-trimethyl-(1-methyl-2-phenyl-ethyl)-ammonium; iodide 
• 50-00-0 formaldehyd 
• 60-15-1 2-amino-1-phenylpropane 
• 103-79-7 1-phenyl-acetone 
• 156-34-3 l-amphetamine 
• 51-64-9 dexamfetamine 
• 4075-96-1 1-phenyl-2-dimethylaminopropane 
• 15351-09-4 metamfepramone 
• 35026-77-8 (S)-2-(dimethylamino)propiophenone 
• 676-58-4 methylmagnesium chloride 
• 68-12-2 N,N-dimethyl-formamide 
• 6921-34-2 benzylmagnesium chloride 
• 88913-09-1 Famprofazon N-oxide 
• 87968-04-5 2-chloro-N,N-dimethyl-3-phenylpropanamide 

Downstream Products

• 14352-83-1 Dimethyl-phenaethyl-<β-phenyl-isopropyl>-ammoniumbromid 
• 14352-86-4 Dimethyl-<β-phenyl-isopropyl>-<3-methyl-buten-(2)-yl>-ammoniumchlorid 
• 98154-55-3 (1S,2S)-N,N-dimethyl-2-methylamphetamine 
• 69792-61-6 N,N-dimethyl-1-(4-hydroxyphenyl)-2-propylamine 
• 14352-80-8 Dimethyl-<β-phenyl-isopropyl>-<3-chlor-buten-(2)-yl>-ammoniumchlorid 
• 24144-22-7 (CH₃)2(C₆H₅CH₂CHCH₃)NBH₃ 
• 98243-47-1 (1S,2S)-2-deuterio-N,N-dimethylamphetamine 
• 116588-21-7 (1S,2S)-2-(Dimethylamino)-1-phenyl-1-(phenylthio)propane 

Relevant articles and documents

Synthesis of tertiary sec-alkylamines by the addition of grignard reagents to N,N-dialkylformamides mediated by Ti(OiPr)4 and Me3SiCl

A number of tertiary sec-alkylamines (22 examples, 29-80% yield) have been prepared according to a simple one-pot procedure by the addition of Grignard reagents to N,N-dialkylformamides in the presence of Ti(OiPr)4 and Me3SiCl. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

Selection of a Sommelet-Hauser or a Stevens Rearrangement Pathway of N,N-Dimethyl(substituted benzyl)ammonium N-Alkylides

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Carbon-13 nuclear magnetic resonance spectra of fentanyl analogs

Natural abundance carbon-13 chemical shifts are reported for the hydrochloride salts of fentanyl and fifteen analogs. The signals are assigned on the basis of chemical shift theory, SFORD multiplicities, signal intensities, comparisons with model compounds, and thiophene carbon-proton coupling constants. In addition to its forensic value, the data suggest that the solution conformations of the analogs are similar to that of fentanyl hydrochloride.