41684-13-3

Basic information

• Product Name: N-[1-(4-methoxyphenyl)ethyl]-N-methylamine
• Synonyms: N-[1-(4-methoxyphenyl)ethyl]-N-methylamine;1-(4-METHOXYPHENYL)-N-METHYLETHANAMINE;AKOS BBV-007891;OTAVA-BB 1146337;1-(4-methoxyphenyl)-N-methylethanamine(SALTDATA: HCl)
• CAS NO: 41684-13-3
• Molecular Formula: C₁₀H₁₅NO
• Molecular Weight: 165.23
• Mol File: 41684-13-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 233.7°C at 760 mmHg
• Flash Point: 92.6°C
• Appearance: /
• Density: 0.958g/cm³
• Vapor Pressure: 0.0551mmHg at 25°C
• Refractive Index: 1.5
• CAS DataBase Reference: N-[1-(4-methoxyphenyl)ethyl]-N-methylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-[1-(4-methoxyphenyl)ethyl]-N-methylamine(41684-13-3)
• EPA Substance Registry System: N-[1-(4-methoxyphenyl)ethyl]-N-methylamine(41684-13-3)

Safety Data

• Hazardous Substances Data: 41684-13-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H15NO/c1-8(11-2)9-4-6-10(12-3)7-5-9/h4-8,11H,1-3H3

Upstream product

• 118761-91-4 N-methyl-[1-(4'-methoxylphenyl)ethylidene]amine 
• 637-69-4 4-Methoxystyrene 
• 41879-39-4 O-(tert-butyldimethylsilanyl)hydroxylamine 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 6298-96-0 1-(4-methoxyphenyl)ethanamine 
• 74-89-5 methylamine 
• 768-60-5 4-methoxyphenylacetylen 
• 83834-91-7 N-formyl 1-(4-methoxyphenyl)ethylamine 

Downstream Products

• 916165-89-4 [2,3,4,5-Ph4(η4-C4CO)Ru(CO)2NH(Me)(CHCH3Ph)] 
• 916165-93-0 [2,3,4,5-Ph4(η4-C4CO)Ru(CO)2NH(Me)(CH(4-MeO-Ph)CH3)] 
• 133302-67-7 4-methoxy-N-methyl-N-(trimethylsilylmethyl)-α-methylbenzylamine 

Relevant articles and documents

Oxidation Under Reductive Conditions: From Benzylic Ethers to Acetals with Perfect Atom-Economy by Titanocene(III) Catalysis

Described here is a titanocene-catalyzed reaction for the synthesis of acetals and hemiaminals from benzylic ethers and benzylic amines, respectively, with pendant epoxides. The reaction proceeds by catalysis in single-electron steps. The oxidative addition comprises an epoxide opening. An H-atom transfer, to generate a benzylic radical, serves as a radical translocation step, and an organometallic oxygen rebound as a reductive elimination. The reaction mechanism was studied by high-level dispersion corrected hybrid functional DFT with implicit solvation. The low-energy conformational space was searched by the efficient CREST program. The stereoselectivity was deduced from the lowest lying benzylic radical structures and their conformations are controlled by hyperconjugative interactions and steric interactions between the titanocene catalyst and the aryl groups of the substrate. An interesting mechanistic aspect is that the oxidation of the benzylic center occurs under reducing conditions.

Structure-Reactivity Relationships on Substrates and Inhibitors of the Lysine Deacylase Sirtuin 2 from Schistosoma mansoni (SmSirt2)

The only drug currently available for treatment of the neglected disease Schistosomiasis is Praziquantel, and the possible emergence of resistance makes research on novel therapeutic agents necessary and urgent. To this end, the targeting of Schistosoma m

Ind2TiMe2-catalyzed addition of methyl- and ethylamine to alkynes

We describe a very simple hydrogenation-like experimental protocol for the addition of gaseous methyl- and ethylamine to alkynes in the presence of Ind2TiMe2 as the catalyst. For efficient hydroamination reactions it is sufficient to stir a mixture of the alkyne and the catalyst in toluene at temperatures between 80°C (terminal alkynes) and 105°C (internal alkynes) under a constant pressure of 1 atm of the corresponding amine. After subsequent reduction of the initially formed imines, methyl- and ethylamine derivatives are the final products of the described one-pot reaction sequences. In the case of 2-alkyl-1-phenylalkynes as starting materials, biologically interesting 2-phenylethylamine derivatives possessing a small methyl or ethyl substituent at the N atom are easily accessible by the new reaction protocol. Wiley-VCH Verlag GmbH & Co. KGaA, 2005.