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3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride

Base Information Edit
  • Chemical Name:3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride
  • CAS No.:1441168-30-4
  • Molecular Formula:C15H20FN*ClH
  • Molecular Weight:269.79
  • Hs Code.:
  • Mol file:1441168-30-4.mol
3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride

Synonyms:3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride

Suppliers and Price of 3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride Edit
Chemical Property:
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Technology Process of 3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride

There total 7 articles about 3-fluoro-N-((2,5,5-trimethylcyclopent-1-enyl)methyl)aniline hydrochloride 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 hydrogenchloride; In diethyl ether; at 20 ℃; for 0.25h;
Guidance literature:
Multi-step reaction with 7 steps
1: hydrogenchloride / methanol; water / 1 h / pH 1 / Reflux
2: zinc(II) iodide / dichloromethane / 4 h / 20 °C
3: hydrogenchloride / tetrahydrofuran; water / 4 h / 45 °C
4: thionyl chloride / 84 °C / Sealed tube
5: diisobutylaluminium hydride / hexane / 2 h / -78 °C / Inert atmosphere
6: acetic acid; sodium cyanoborohydride / methanol / 20 °C
7: hydrogenchloride / diethyl ether / 0.25 h / 20 °C
With hydrogenchloride; thionyl chloride; diisobutylaluminium hydride; sodium cyanoborohydride; acetic acid; zinc(II) iodide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water;
Guidance literature:
Multi-step reaction with 6 steps
1: zinc(II) iodide / dichloromethane / 4 h / 20 °C
2: hydrogenchloride / tetrahydrofuran; water / 4 h / 45 °C
3: thionyl chloride / 84 °C / Sealed tube
4: diisobutylaluminium hydride / hexane / 2 h / -78 °C / Inert atmosphere
5: acetic acid; sodium cyanoborohydride / methanol / 20 °C
6: hydrogenchloride / diethyl ether / 0.25 h / 20 °C
With hydrogenchloride; thionyl chloride; diisobutylaluminium hydride; sodium cyanoborohydride; acetic acid; zinc(II) iodide; In tetrahydrofuran; methanol; diethyl ether; hexane; dichloromethane; water;
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