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(+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde

Base Information Edit
  • Chemical Name:(+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde
  • CAS No.:110654-72-3
  • Molecular Formula:C21H30O2S2
  • Molecular Weight:378.6
  • Hs Code.:
  • Mol file:110654-72-3.mol
(+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde

Synonyms:(+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde

Suppliers and Price of (+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde
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Chemical Property of (+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde Edit
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Technology Process of (+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde

There total 4 articles about (+/-)-(1RS,2SR)-5,5-ethylenedithio-2-<2-(2-methoxyphenyl)ethyl>-1,3,3-trimethylcyclohexanecarbaldehyde 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 3 steps
1: 71 percent / triethylaluminium / tetrahydrofuran / 22 h / Ambient temperature
2: 92 percent / boron trifluoride-diethyl ether / CH2Cl2 / 5 h / Ambient temperature
3: 1.) DIBAL; 2.) aq. HCl / 1.) DME, reflux, 2 h; 2.) reflux, 2 h.
With hydrogenchloride; boron trifluoride diethyl etherate; triethylaluminum; diisobutylaluminium hydride; In tetrahydrofuran; dichloromethane;
Guidance literature:
Multi-step reaction with 4 steps
1: 1.) copper(I)bromide; 2.) aq. HCl / 1.) diethyl ether, THF, 0 deg C; rt, 0.5 h; 2.)THF, reflux, 2 h.
2: 71 percent / triethylaluminium / tetrahydrofuran / 22 h / Ambient temperature
3: 92 percent / boron trifluoride-diethyl ether / CH2Cl2 / 5 h / Ambient temperature
4: 1.) DIBAL; 2.) aq. HCl / 1.) DME, reflux, 2 h; 2.) reflux, 2 h.
With hydrogenchloride; boron trifluoride diethyl etherate; triethylaluminum; diisobutylaluminium hydride; copper(I) bromide; In tetrahydrofuran; dichloromethane;
Guidance literature:
Multi-step reaction with 2 steps
1: 92 percent / boron trifluoride-diethyl ether / CH2Cl2 / 5 h / Ambient temperature
2: 1.) DIBAL; 2.) aq. HCl / 1.) DME, reflux, 2 h; 2.) reflux, 2 h.
With hydrogenchloride; boron trifluoride diethyl etherate; diisobutylaluminium hydride; In dichloromethane;
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