71126-62-0

Basic information

• Product Name: N-Methyl-2-(phenylmethoxy)-ethanamine
• Synonyms: N-Methyl-2-(phenylmethoxy)-ethanamine;2-(benzyloxy)-N-methylethan-1-amine;Ethanamine, N-methyl-2-(phenylmethoxy)-
• CAS NO: 71126-62-0
• Molecular Formula: C₁₀H₁₅NO
• Molecular Weight: 165.2322
• Mol File: 71126-62-0.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 229.1°Cat760mmHg
• Flash Point: 90.8°C
• Appearance: /
• Density: 0.969g/cm³
• Vapor Pressure: 0.0707mmHg at 25°C
• Refractive Index: 1.503
• PKA: 9.57±0.10(Predicted)
• CAS DataBase Reference: N-Methyl-2-(phenylmethoxy)-ethanamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-Methyl-2-(phenylmethoxy)-ethanamine(71126-62-0)
• EPA Substance Registry System: N-Methyl-2-(phenylmethoxy)-ethanamine(71126-62-0)

Safety Data

• Hazardous Substances Data: 71126-62-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H15NO/c1-11-7-8-12-9-10-5-3-2-4-6-10/h2-6,11H,7-9H2,1H3

Upstream product

• 17229-17-3 benzyl 2-chloroethyl ether 
• 74-89-5 methylamine 
• 54555-84-9 benzyl iodoethyl ether 
• 100-39-0 benzyl bromide 
• 60656-87-3 benzyloxyacetoaldehyde 
• 27058-15-7 N-benzyl-2-(benzyloxy)-N-methylethan-1-amine 

Downstream Products

• 168274-64-4 1-(2-benzyloxyethyl)-4,4-dideuteroimidazolidin-2-one 
• 66046-66-0 2-[(2-benzyloxy-ethyl)-methyl-amino]-3-(2-chloro-ethyl)-2-oxo-2λ⁵-[1,3,2]oxazaphosphinan-4-one 
• 883973-47-5 2-[3-(2-benzyloxy-ethyl)-3-methyl-ureido]-N-methoxy-N-methyl-3-phenyl-propionamide 
• 883973-36-2 (S)-2-[3-(2-Benzyloxy-ethyl)-3-methyl-ureido]-3-phenyl-propionic acid 
• 883973-92-0 (S)-2-[3-(2-Benzyloxy-ethyl)-3-methyl-ureido]-3-phenyl-propionic acid methyl ester 
• 66046-63-7 N-(2-benzyloxy-ethyl)-N'-(2-chloro-ethyl)-N-methyl-phosphorodiamidic acid but-3-enyl ester 

Relevant articles and documents

Synthesis of Diverse N-Acryloyl Azetidines and Evaluation of Their Enhanced Thiol Reactivities

Acyl azetidines exhibit nonplanar hybridization, leading to lower amide-like character of the corresponding (O)C-N bonds. This impacts N-acryloyl azetidines by producing enhanced electrophilicy at appended Michael acceptors. Herein, reactivity data are reported in the presence of glutathione (GSH) in phosphate buffer (pH 7.4) at 37 °C. Wide reactivity ranges are observed by varying substitution at the Michael acceptor or by modulating the electron-withdrawing character of substituents at the C3 position of the azetidine.

QUINOLONE DERIVATIVES AS FIBROBLAST GROWTH FACTOR RECEPTOR INHIBITORS

Compounds that are Fibroblast Growth Factor Inhibitors (FGFR) and are therefore useful for the treatment of diseases treatable by inhibition of FGFR are disclosed. Also disclosed are pharmaceutical compositions containing such compounds and processes for

Chemoselective deprotection of teriary benzylamines and reduction of carbon-carbon double bonds in the presence of benzyl and benzyloxymethyl ethers

Catalytic transfer hydrogenation using 10% Pd-C in the presence of 1,4-cyclohexadiene as the hydrogen donor selectively debenzylates amines and reduces carbon-carbon double bonds while leaving benzyl and benzyloxymethyl ethers intact. (C) 2000 Elsevier Sc