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N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine

Base Information
  • Chemical Name:N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine
  • CAS No.:404-50-2
  • Molecular Formula:C15H16FN
  • Molecular Weight:229.297
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80402402
  • Wikidata:Q82205809
  • Mol file:404-50-2.mol
N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine

Synonyms:N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine;404-50-2;N-Benzyl-4-fluoro-N-MethylbenzylaMine;N-[(4-fluorophenyl)methyl]-N-methyl-1-phenylmethanamine;SCHEMBL21268450;DTXSID80402402;STK113013;AKOS017093702;SB80432;NCGC00479725-01;N-Benzyl-4-fluoro-N-methylbenzylamine,97%;BENZYL[(4-FLUOROPHENYL)METHYL]METHYLAMINE

Suppliers and Price of N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine
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
  • Crysdot
  • N-Benzyl-1-(4-fluorophenyl)-N-methylmethanamine 95+%
  • 5g
  • $ 671.00
  • Alichem
  • N-Benzyl-1-(4-fluorophenyl)-N-methylmethanamine
  • 1g
  • $ 400.00
Total 11 raw suppliers
Chemical Property of N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine
Chemical Property:
  • PSA:3.24000 
  • LogP:3.45770 
  • Storage Temp.:2-8°C 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:4
  • Exact Mass:229.126677677
  • Heavy Atom Count:17
  • Complexity:205
Purity/Quality:

97% *data from raw suppliers

N-Benzyl-1-(4-fluorophenyl)-N-methylmethanamine 95+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN(CC1=CC=CC=C1)CC2=CC=C(C=C2)F
Technology Process of N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine

There total 4 articles about N-benzyl-1-(4-fluorophenyl)-N-methylmethanamine 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 C25H27ClIrN4(1+)*Cl(1-); caesium carbonate; at 125 ℃; for 12h; Schlenk technique;
DOI:10.1016/j.jcat.2021.08.037
Guidance literature:
4-fluorobenzaldehyde; benzyl-methyl-amine; With ammonium hexafluorophosphate; In methanol; at 100 ℃; for 3h; Autoclave; Inert atmosphere;
With trimethylamine-N-oxide; (1,4-dimethyl-5,7-diphenyl-1,2,3,4-tetrahydro-6H-cyclopenta[b]pyrazin-6-one) irontricarbonyl complex3; hydrogen; In methanol; at 44 ℃; for 16h; under 3750.38 Torr; Reagent/catalyst; Autoclave;
DOI:10.1002/chem.201500720
Guidance literature:
With hydrogen; In hexane; at 170 ℃; for 7h; under 15001.5 - 45004.5 Torr; Autoclave; Green chemistry;
DOI:10.1002/cssc.201500486
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