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[(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide

Base Information
  • Chemical Name:[(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide
  • CAS No.:75210-06-9
  • Molecular Formula:BrH*C26H35NO
  • Molecular Weight:458.482
  • Hs Code.:
[(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide

Synonyms:

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Chemical Property of [(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide
Chemical Property:
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Technology Process of [(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide

There total 15 articles about [(1R,6S,10S)-1-(3-Methoxy-phenyl)-bicyclo[4.3.1]dec-10-yl]-methyl-phenethyl-amine; hydrobromide 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 15 steps
1: 1.) Mg / 1.) THF, 2.) THF, room temp., 30 min, 50-55 deg C, 1 h
2: oxalic acid / toluene / 16 h / Heating
3: 1.) NaBH4, BF3*Et2O, 2.) 10percent NaOH, 30percent H2O2 / 1.) THF, room temp., 15 h, 2.) THF, H2O, room temp., 1 h
4: 33.6 percent / Na2Cr2O7*2H2O, conc. H2SO4 / diethyl ether; H2O / 2 h / 5 - 13 °C
5: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
6: 78 percent / benzene / 20 h / Heating
7: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
8: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
9: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
10: 80.2 percent / pyridine / 4 h / Ambient temperature
11: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
12: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
13: LiAlH4 / diethyl ether / 8 h / Heating
14: K2CO3 / tetrahydrofuran; H2O / Ambient temperature
15: 1.) NaBH4, BF3*Et2O, 2.) 23percent HCl, 3.) HBr / 1.) THF, room temp., 2.) EtOH, Et2O, room temp.
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium dichromate; sulfuric acid; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen bromide; hydrogen; dihydrogen peroxide; sodium acetate; oxalic acid; titanium tetrachloride; sodium hydrogencarbonate; potassium carbonate; magnesium; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1248/cpb.28.1022
Guidance literature:
Multi-step reaction with 14 steps
1: oxalic acid / toluene / 16 h / Heating
2: 1.) NaBH4, BF3*Et2O, 2.) 10percent NaOH, 30percent H2O2 / 1.) THF, room temp., 15 h, 2.) THF, H2O, room temp., 1 h
3: 33.6 percent / Na2Cr2O7*2H2O, conc. H2SO4 / diethyl ether; H2O / 2 h / 5 - 13 °C
4: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
5: 78 percent / benzene / 20 h / Heating
6: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
7: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
8: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
9: 80.2 percent / pyridine / 4 h / Ambient temperature
10: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
11: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
12: LiAlH4 / diethyl ether / 8 h / Heating
13: K2CO3 / tetrahydrofuran; H2O / Ambient temperature
14: 1.) NaBH4, BF3*Et2O, 2.) 23percent HCl, 3.) HBr / 1.) THF, room temp., 2.) EtOH, Et2O, room temp.
With hydrogenchloride; sodium hydroxide; sodium tetrahydroborate; lithium aluminium tetrahydride; sodium dichromate; sulfuric acid; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen bromide; hydrogen; dihydrogen peroxide; sodium acetate; oxalic acid; titanium tetrachloride; sodium hydrogencarbonate; potassium carbonate; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1248/cpb.28.1022
Guidance literature:
Multi-step reaction with 11 steps
1: 75.8 percent / TiCl4 / benzene / 1.) room temp., overnight, 2.) 75-80 deg C, 8 h
2: 78 percent / benzene / 20 h / Heating
3: 90.3 percent / NH2OH*HCl, NaOAc / dimethylformamide / Ambient temperature
4: 81.9 percent / LiAlH4 / tetrahydrofuran; dioxane / Heating
5: 73.3 percent / 5percent NaHCO3 / CH2Cl2 / 4 h / Ambient temperature
6: 80.2 percent / pyridine / 4 h / Ambient temperature
7: 44.3 percent / NaI, Zn / 1,2-dimethoxy-ethane / 76 h / Heating
8: 97.7 percent / H2 / 10percent Pd-C / ethanol / 7.5 h / 70 - 90 °C / 47808 Torr
9: LiAlH4 / diethyl ether / 8 h / Heating
10: K2CO3 / tetrahydrofuran; H2O / Ambient temperature
11: 1.) NaBH4, BF3*Et2O, 2.) 23percent HCl, 3.) HBr / 1.) THF, room temp., 2.) EtOH, Et2O, room temp.
With hydrogenchloride; sodium tetrahydroborate; lithium aluminium tetrahydride; boron trifluoride diethyl etherate; hydroxylamine hydrochloride; hydrogen bromide; hydrogen; sodium acetate; titanium tetrachloride; sodium hydrogencarbonate; potassium carbonate; sodium iodide; zinc; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; pyridine; 1,2-dimethoxyethane; diethyl ether; ethanol; dichloromethane; water; N,N-dimethyl-formamide; benzene;
DOI:10.1248/cpb.28.1022
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