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(+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin

Base Information Edit
  • Chemical Name:(+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin
  • CAS No.:76441-49-1
  • Molecular Formula:C11H17NS
  • Molecular Weight:195.329
  • Hs Code.:
  • Mol file:76441-49-1.mol
(+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin

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Chemical Property of (+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin Edit
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Technology Process of (+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin

There total 19 articles about (+)-cis-2-Methyl-2-(3-thienyl)-1-cyclohexylamin 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 9 steps
1: diethyl ether / 2 h / -70 °C
2: oxalic acid / toluene
3: 52.4 percent / amyl nitrite, 30percent aq. HCl / 3 h / -10 °C
4: 45.8 percent / 1.) pyridine / 1.) 70 deg C, 2.5 h, 2.) room temp., 15 h
5: 82.5 percent / 10percent aq. H2SO4 / 1.5 h / Heating
6: 99 percent / H2 / Pd/C / dioxane / 0.25 h
7: 100 percent / 1.) NaH / 1.) benzene, reflux, 5 h, 2.) 45 deg C, 15 h
8: 71 percent / NH2OH*HCl, NaAc / aq. ethanol / 0.67 h
9: LiAlH4 / tetrahydrofuran / 15 h / Heating
With pyridine; hydrogenchloride; lithium aluminium tetrahydride; n-Amyl nitrite; sulfuric acid; hydroxylamine hydrochloride; hydrogen; sodium acetate; oxalic acid; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; toluene;
DOI:10.1002/ardp.19803131011
Guidance literature:
Multi-step reaction with 9 steps
1: diethyl ether / 2 h / -70 °C
2: oxalic acid / toluene
3: 52.4 percent / amyl nitrite, 30percent aq. HCl / 3 h / -10 °C
4: 45.8 percent / 1.) pyridine / 1.) 70 deg C, 2.5 h, 2.) room temp., 15 h
5: 82.5 percent / 10percent aq. H2SO4 / 1.5 h / Heating
6: 99 percent / H2 / Pd/C / dioxane / 0.25 h
7: 100 percent / 1.) NaH / 1.) benzene, reflux, 5 h, 2.) 45 deg C, 15 h
8: 71 percent / NH2OH*HCl, NaAc / aq. ethanol / 0.67 h
9: LiAlH4 / tetrahydrofuran / 15 h / Heating
With pyridine; hydrogenchloride; lithium aluminium tetrahydride; n-Amyl nitrite; sulfuric acid; hydroxylamine hydrochloride; hydrogen; sodium acetate; oxalic acid; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; diethyl ether; ethanol; toluene;
DOI:10.1002/ardp.19803131011
Guidance literature:
Multi-step reaction with 7 steps
1: 52.4 percent / amyl nitrite, 30percent aq. HCl / 3 h / -10 °C
2: 45.8 percent / 1.) pyridine / 1.) 70 deg C, 2.5 h, 2.) room temp., 15 h
3: 82.5 percent / 10percent aq. H2SO4 / 1.5 h / Heating
4: 99 percent / H2 / Pd/C / dioxane / 0.25 h
5: 100 percent / 1.) NaH / 1.) benzene, reflux, 5 h, 2.) 45 deg C, 15 h
6: 71 percent / NH2OH*HCl, NaAc / aq. ethanol / 0.67 h
7: LiAlH4 / tetrahydrofuran / 15 h / Heating
With pyridine; hydrogenchloride; lithium aluminium tetrahydride; n-Amyl nitrite; sulfuric acid; hydroxylamine hydrochloride; hydrogen; sodium acetate; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; ethanol;
DOI:10.1002/ardp.19803131011
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