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N-(3-Fluorobenzyl)-4-Methoxyaniline, 97%

Base Information Edit
  • Chemical Name:N-(3-Fluorobenzyl)-4-Methoxyaniline, 97%
  • CAS No.:415968-77-3
  • Molecular Formula:C14H14FNO
  • Molecular Weight:231.27
  • Hs Code.:
  • Mol file:415968-77-3.mol
N-(3-Fluorobenzyl)-4-Methoxyaniline, 97%

Synonyms:N-(3-fluorobenzyl)-4-methoxyaniline

Suppliers and Price of N-(3-Fluorobenzyl)-4-Methoxyaniline, 97%
Supply Marketing:Edit
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
  • Matrix Scientific
  • N-[(3-Fluorophenyl)methyl]-4-methoxyaniline
  • 5g
  • $ 1320.00
  • A1 Biochem Labs
  • N-[(3-Fluorophenyl)methyl]-4-methoxyaniline 95%
  • 5 g
  • $ 800.00
Total 1 raw suppliers
Chemical Property of N-(3-Fluorobenzyl)-4-Methoxyaniline, 97% Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

N-[(3-Fluorophenyl)methyl]-4-methoxyaniline *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of N-(3-Fluorobenzyl)-4-Methoxyaniline, 97%

There total 2 articles about N-(3-Fluorobenzyl)-4-Methoxyaniline, 97% 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 triiron dodecarbonyl; hydrogen; In toluene; at 65 ℃; for 24h; under 37503.8 Torr; Autoclave;
DOI:10.1002/asia.201100462
Guidance literature:
With tris(pentafluorophenyl)borate; In toluene; at 120 ℃; for 36h; chemoselective reaction; Molecular sieve; Schlenk technique; Inert atmosphere; Sealed tube;
DOI:10.1021/acs.joc.9b02816
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