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(4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene

Base Information
  • Chemical Name:(4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene
  • CAS No.:108032-54-8
  • Molecular Formula:C12H22O
  • Molecular Weight:182.306
  • Hs Code.:
(4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene

Synonyms:(4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene

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Chemical Property of (4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene
Chemical Property:
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Technology Process of (4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene

There total 12 articles about (4S,6S)-6-(2-Hydroxy)ethyl-1,4,5,5-tetramethylcyclohexene 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 12 steps
1: 97.2 percent / hydroquinone / benzene / 19 h / Heating
2: 1) NaHCO3, 2) KI, I2 / 1) water, 2 h, r.t., 2) water, 17 h, r.t.
3: 4.58 g / BH3*Me2S, B(OMe)3 / tetrahydrofuran / 7 h / Ambient temperature
4: 63 percent / Zn-dust, AcOH / 1 h / 90 °C
5: 1) LDA / 1) THF, -65 deg C, 30 min, 2) -65 deg C, 4 h
6: 77.4 percent / i-Bu2AlH / tetrahydrofuran; toluene / 1 h / -65 °C
7: CSA / benzene / 0.5 h
8: 91.6 percent / TsOH / dioxane; H2O / 1 h / Heating
9: 90.3 percent / NaOH, 80percent N2H4 / bis-(2-hydroxy-ethyl) ether / 1) 35 min, 100 deg C, 2) to 210 deg C, 1 h, 3) 2 h, 210 deg C
10: 94.4 percent / Et3N / CH2Cl2 / 0.5 h / 0 °C
11: 94.4 percent / LiEt3BH / tetrahydrofuran / 1 h / 50 °C
12: 96.7 percent / Na, liq. NH3 / tetrahydrofuran / 1 h
With sodium hydroxide; Trimethyl borate; dimethylsulfide borane complex; camphor-10-sulfonic acid; ammonia; iodine; sodium; diisobutylaluminium hydride; lithium triethylborohydride; sodium hydrogencarbonate; toluene-4-sulfonic acid; hydrazine hydrate; acetic acid; triethylamine; hydroquinone; potassium iodide; zinc; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; toluene; diethylene glycol; benzene;
DOI:10.1248/cpb.39.2540
Guidance literature:
Multi-step reaction with 8 steps
1: 1) LDA / 1) THF, -65 deg C, 30 min, 2) -65 deg C, 4 h
2: 77.4 percent / i-Bu2AlH / tetrahydrofuran; toluene / 1 h / -65 °C
3: CSA / benzene / 0.5 h
4: 91.6 percent / TsOH / dioxane; H2O / 1 h / Heating
5: 90.3 percent / NaOH, 80percent N2H4 / bis-(2-hydroxy-ethyl) ether / 1) 35 min, 100 deg C, 2) to 210 deg C, 1 h, 3) 2 h, 210 deg C
6: 94.4 percent / Et3N / CH2Cl2 / 0.5 h / 0 °C
7: 94.4 percent / LiEt3BH / tetrahydrofuran / 1 h / 50 °C
8: 96.7 percent / Na, liq. NH3 / tetrahydrofuran / 1 h
With sodium hydroxide; camphor-10-sulfonic acid; ammonia; sodium; diisobutylaluminium hydride; lithium triethylborohydride; toluene-4-sulfonic acid; hydrazine hydrate; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; toluene; diethylene glycol; benzene;
DOI:10.1248/cpb.39.2540
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