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2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene

Base Information
  • Chemical Name:2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene
  • CAS No.:81482-27-1
  • Molecular Formula:C23H34O5
  • Molecular Weight:390.52
  • Hs Code.:
2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene

Synonyms:

Suppliers and Price of 2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene
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Chemical Property of 2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene
Chemical Property:
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Technology Process of 2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene

There total 10 articles about 2(2-ethyloxy-5-ethylenedioxycyclohexyl)-1,3-dimethoxy-5-pentylbenzene 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 10 steps
1: n-BuLi
2: 87 percent / piperidine
3: 99 percent / benzene / 2 h / Heating
4: 94 percent / 6N hydrochloric acid / acetone / 0.75 h / Ambient temperature
5: 91 percent / p-toluenesulfonic acid / benzene / 2.5 h / Heating
6: 99 percent / 10percent palladium on charcoal, hydrogen / ethanol / 6 h
7: 93 percent / p-toluenesulfonic acid / benzene / 4 h / Heating
8: 94 percent / 10N aqueous sodium hydroxide / ethanol / 20 h / Heating
9: 88 percent / sodium hydroxide / dimethylformamide / 8 h / Heating
10: 40 percent / diethyl ether / 6 h / Heating
With piperidine; hydrogenchloride; sodium hydroxide; palladium on activated charcoal; n-butyllithium; hydrogen; toluene-4-sulfonic acid; In diethyl ether; ethanol; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1139/v82-047
Guidance literature:
Multi-step reaction with 9 steps
1: 87 percent / piperidine
2: 99 percent / benzene / 2 h / Heating
3: 94 percent / 6N hydrochloric acid / acetone / 0.75 h / Ambient temperature
4: 91 percent / p-toluenesulfonic acid / benzene / 2.5 h / Heating
5: 99 percent / 10percent palladium on charcoal, hydrogen / ethanol / 6 h
6: 93 percent / p-toluenesulfonic acid / benzene / 4 h / Heating
7: 94 percent / 10N aqueous sodium hydroxide / ethanol / 20 h / Heating
8: 88 percent / sodium hydroxide / dimethylformamide / 8 h / Heating
9: 40 percent / diethyl ether / 6 h / Heating
With piperidine; hydrogenchloride; sodium hydroxide; palladium on activated charcoal; hydrogen; toluene-4-sulfonic acid; In diethyl ether; ethanol; N,N-dimethyl-formamide; acetone; benzene;
DOI:10.1139/v82-047
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