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trans-4-cyclohexyl-4-methoxybenzoat

Base Information
  • Chemical Name:trans-4-cyclohexyl-4-methoxybenzoat
  • CAS No.:110568-52-0
  • Molecular Formula:C29H44O3
  • Molecular Weight:440.667
  • Hs Code.:
trans-4-<trans-4-(trans-4-Propylcyclohexyl)cyclohexyl>cyclohexyl-4-methoxybenzoat

Synonyms:

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Chemical Property of trans-4-cyclohexyl-4-methoxybenzoat
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Technology Process of trans-4-cyclohexyl-4-methoxybenzoat

There total 12 articles about trans-4-cyclohexyl-4-methoxybenzoat 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 13 steps
1: ethyl acetate / 0.5 h / Ambient temperature
2: 35 percent H2O2 / ethyl acetate; tetrahydrofuran / 1 h / Ambient temperature
3: 72 percent / LiAlH4 / diethyl ether / 1 h / Ambient temperature
4: 83 percent / tert-butylhydroperoxide, VO(acac)2 / benzene / 48 h / 40 °C
5: 99 percent / CrO3, pyridine / CH2Cl2 / 0.25 h / Ambient temperature
6: 66 percent / hydrazin hydrate, glacial acetic acid / ethanol / 1.5 h / Ambient temperature
7: 88 percent / 4-methylmorpholine / diethyl ether / 20 h / Ambient temperature
8: 91 percent / lithium iodide hydrate / dimethylformamide / 1 h / Heating
9: 94 percent / H2 / Pt-oxide / ethyl acetate / 1 h
10: 83 percent / K2CO3 / diethyl ether / 16 h / Ambient temperature
11: 95 percent / 2) HCl (5 percent) / benzene / 1) 6 h, 60 deg C; 2) 30 min, r.t.
12: 55 percent / 2 N NaOH / benzene / 3 h / Heating
13: pyridine / 3 h / Ambient temperature
With 4-methyl-morpholine; pyridine; chromium(VI) oxide; hydrogenchloride; tert.-butylhydroperoxide; sodium hydroxide; lithium aluminium tetrahydride; bis(acetylacetonate)oxovanadium; hydrogen; dihydrogen peroxide; potassium carbonate; hydrazine hydrate; acetic acid; lithium iodide; Pt-oxide; In tetrahydrofuran; pyridine; diethyl ether; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; benzene;
Guidance literature:
Multi-step reaction with 9 steps
1: 99 percent / CrO3, pyridine / CH2Cl2 / 0.25 h / Ambient temperature
2: 66 percent / hydrazin hydrate, glacial acetic acid / ethanol / 1.5 h / Ambient temperature
3: 88 percent / 4-methylmorpholine / diethyl ether / 20 h / Ambient temperature
4: 91 percent / lithium iodide hydrate / dimethylformamide / 1 h / Heating
5: 94 percent / H2 / Pt-oxide / ethyl acetate / 1 h
6: 83 percent / K2CO3 / diethyl ether / 16 h / Ambient temperature
7: 95 percent / 2) HCl (5 percent) / benzene / 1) 6 h, 60 deg C; 2) 30 min, r.t.
8: 55 percent / 2 N NaOH / benzene / 3 h / Heating
9: pyridine / 3 h / Ambient temperature
With 4-methyl-morpholine; pyridine; chromium(VI) oxide; hydrogenchloride; sodium hydroxide; hydrogen; potassium carbonate; hydrazine hydrate; acetic acid; lithium iodide; Pt-oxide; In pyridine; diethyl ether; ethanol; dichloromethane; ethyl acetate; N,N-dimethyl-formamide; benzene;
Guidance literature:
Multi-step reaction with 7 steps
1: 88 percent / 4-methylmorpholine / diethyl ether / 20 h / Ambient temperature
2: 91 percent / lithium iodide hydrate / dimethylformamide / 1 h / Heating
3: 94 percent / H2 / Pt-oxide / ethyl acetate / 1 h
4: 83 percent / K2CO3 / diethyl ether / 16 h / Ambient temperature
5: 95 percent / 2) HCl (5 percent) / benzene / 1) 6 h, 60 deg C; 2) 30 min, r.t.
6: 55 percent / 2 N NaOH / benzene / 3 h / Heating
7: pyridine / 3 h / Ambient temperature
With 4-methyl-morpholine; hydrogenchloride; sodium hydroxide; hydrogen; potassium carbonate; lithium iodide; Pt-oxide; In pyridine; diethyl ether; ethyl acetate; N,N-dimethyl-formamide; benzene;
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