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N-(4-Methoxybenzyl)-N-methylamine

Base Information
  • Chemical Name:N-(4-Methoxybenzyl)-N-methylamine
  • CAS No.:702-24-9
  • Molecular Formula:C9H13NO
  • Molecular Weight:151.208
  • Hs Code.:2922299090
  • European Community (EC) Number:662-855-1
  • DSSTox Substance ID:DTXSID80220466
  • Nikkaji Number:J971.867B
  • Wikidata:Q72489300
  • ChEMBL ID:CHEMBL1178119
  • Mol file:702-24-9.mol
N-(4-Methoxybenzyl)-N-methylamine

Synonyms:702-24-9;4-Methoxy-N-methylbenzylamine;N-(4-Methoxybenzyl)-N-methylamine;N-Methyl-4-methoxybenzylamine;1-(4-methoxyphenyl)-N-methylmethanamine;Benzenemethanamine, 4-methoxy-N-methyl-;(4-Methoxy-benzyl)-methyl-amine;(4-methoxyphenyl)-N-methylmethanamine;[(4-methoxyphenyl)methyl](methyl)amine;MFCD04115407;4-(Methoxybenzyl)-N-methylamine;N-Methyl-p-methoxybenzylamine;1-(4-methoxyphenyl)-N-methyl-methanamine;SCHEMBL9831;methyl-4-methoxybenzyl amine;4-methoxy-N-methylbenzyl amine;N-(4-Methoxybenzyl)methylamine;CHEMBL1178119;DTXSID80220466;HMS1729L05;CS-D0566;4-methoxy-N-methylbenzenemethanamine;BBL100305;STL553920;AKOS000263995;AS-5663;SB76683;NCGC00374053-01;SY002786;AM20050324;BB 0218330;FT-0629233;M2836;EN300-06567;N-(4-methoxybenzyl)-N-Methylamine, AldrichCPR;J-501424;Z56928625;N-(4-Methoxybenzyl)-N-methylamine, 4-[(Methylamino)methyl]anisole

Suppliers and Price of N-(4-Methoxybenzyl)-N-methylamine
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • N-(4-Methoxybenzyl)-N-methylamine
  • 1g
  • $ 50.00
  • TCI Chemical
  • 4-Methoxy-N-methylbenzylamine >98.0%(GC)(T)
  • 5g
  • $ 87.00
  • TCI Chemical
  • 4-Methoxy-N-methylbenzylamine >98.0%(GC)(T)
  • 1g
  • $ 30.00
  • SynQuest Laboratories
  • 4-Methoxy-N-methylbenzylamine
  • 250 mg
  • $ 32.00
  • SynQuest Laboratories
  • 4-Methoxy-N-methylbenzylamine
  • 1 g
  • $ 116.00
  • SynQuest Laboratories
  • 4-Methoxy-N-methylbenzylamine
  • 5 g
  • $ 205.00
  • SynChem
  • 4-Methoxy-N-methylbenzylamine 95+%
  • 10 g
  • $ 125.00
  • SynChem
  • 4-Methoxy-N-methylbenzylamine 95+%
  • 5 g
  • $ 70.00
  • SynChem
  • 4-Methoxy-N-methylbenzylamine 95+%
  • 1 g
  • $ 25.00
  • Sigma-Aldrich
  • 4-Methoxy-N-methylbenzylamine
  • 1g
  • $ 54.90
Total 79 raw suppliers
Chemical Property of N-(4-Methoxybenzyl)-N-methylamine
Chemical Property:
  • Appearance/Colour:colorless liquid. 
  • Vapor Pressure:0.104mmHg at 25°C 
  • Melting Point:238 °C 
  • Refractive Index:n20/D1.529 
  • Boiling Point:222.035 °C at 760 mmHg 
  • PKA:10.14±0.10(Predicted) 
  • Flash Point:85.118 °C 
  • PSA:21.26000 
  • Density:0.975 g/cm3 
  • LogP:1.80550 
  • Storage Temp.:2-8°C 
  • Solubility.:Chloroform (Slightly), Methanol (Slightly) 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:151.099714038
  • Heavy Atom Count:11
  • Complexity:97.7
Purity/Quality:

99%, *data from raw suppliers

N-(4-Methoxybenzyl)-N-methylamine *data from reagent suppliers

Safty Information:
  • Pictogram(s): Corrosive
  • Hazard Codes:C,Xn 
  • Statements: 36/37/38-34-22 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CNCC1=CC=C(C=C1)OC
  • Uses N-(4-Methoxybenzyl)-N-methylamine is used in the synthetic preparation of many types of compounds, including the synthesis of trifluoromethyl-sulfonimidamides from sulfinamides as well as the preparation of piperazinylquinazoline amine compounds as toll-like receptor 9 signaling antagonists for treatment of immune disorders.
Technology Process of N-(4-Methoxybenzyl)-N-methylamine

There total 40 articles about N-(4-Methoxybenzyl)-N-methylamine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium tetrahydroborate; In ethanol; at 20 ℃; for 20h;
DOI:10.1016/j.bmc.2006.09.026
Guidance literature:
4-methoxy-benzaldehyde; methylamine; In ethanol; at 20 ℃; for 18h;
With sodium tetrahydroborate; In ethanol; for 1.5h;
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1021/jm00357a001
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