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6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one

Base Information Edit
  • Chemical Name:6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one
  • CAS No.:133496-69-2
  • Molecular Formula:C25H28F2N2O2
  • Molecular Weight:426.506
  • Hs Code.:
  • Mol file:133496-69-2.mol
6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one

Synonyms:6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one

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Chemical Property of 6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one Edit
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Technology Process of 6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one

There total 8 articles about 6-Fluoro-3-{4-[4-(4-fluoro-phenyl)-4-oxo-butyl]-piperazin-1-ylmethyl}-3,4-dihydro-2H-naphthalen-1-one 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:
Multi-step reaction with 4 steps
1: glacial acetic acid, 33percent HBr-AcOH / 1.) RT, 15 min, 2.) 80 deg C, 4 h
2: diethyl ether
3: 85 percent / Na2CO3, KI / various solvent(s) / 20 h / Heating
4: 43 percent / polyphosphoric acid / 5 h / 130 °C
With PPA; hydrogen bromide; sodium carbonate; acetic acid; potassium iodide; In diethyl ether;
DOI:10.1021/jm00111a046
Guidance literature:
Multi-step reaction with 3 steps
1: diethyl ether
2: 85 percent / Na2CO3, KI / various solvent(s) / 20 h / Heating
3: 43 percent / polyphosphoric acid / 5 h / 130 °C
With PPA; sodium carbonate; potassium iodide; In diethyl ether;
DOI:10.1021/jm00111a046
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