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1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide

Base Information
  • Chemical Name:1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide
  • CAS No.:141300-60-9
  • Molecular Formula:C27H45BrO4
  • Molecular Weight:513.556
  • Hs Code.:
1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide

Synonyms:1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide

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Chemical Property of 1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide
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Technology Process of 1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide

There total 1 articles about 1α,3β-bis(methoxymethoxy)-21-norchol-5-en-24-yl bromide 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 8 steps
1: 1.) t-BuOK, 3.) pyridine, 4-dimethylaminopyridine
2: 66 percent / diethylaluminum chloride / CH2Cl2; hexane / 24 h / Ambient temperature
3: H2 / 5percent Pt/C / ethyl acetate / 1.5 h / Ambient temperature
4: 85percent KOH / methanol / a) reflux, 6 h, b) RT, 14 h
5: iso-Pr2NEt / tetrahydrofuran; dimethylformamide / 14 h / 45 °C
6: LiAlH4 / tetrahydrofuran / 2 h / Ambient temperature
7: pyridine / 14 h / Ambient temperature
8: LiBr / tetrahydrofuran / 20 h / 50 °C
With pyridine; dmap; potassium hydroxide; lithium aluminium tetrahydride; potassium tert-butylate; hydrogen; diethylaluminium chloride; N-ethyl-N,N-diisopropylamine; lithium bromide; platinum on activated charcoal; In tetrahydrofuran; methanol; hexane; dichloromethane; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1248/cpb.40.648
Guidance literature:
Multi-step reaction with 7 steps
1: 1.) n-BuLi / 1.) THF, n-hexane, 4 deg C, 2 h, 2.) THF, n-hexane, 4 deg C, 1 h
2: 83 percent / CH3I, H2O / acetone / 20 h / Heating
3: 60 percent / tetrahydrofuran / 0.5 h / Ambient temperature
4: 86 percent / 4-dimethylaminopyridine, pyridine / 49 h / Ambient temperature
5: 1.) NBS, NaHCO3, 2.) γ-collidine
6: 34 percent / LiAlH4 / tetrahydrofuran / 1.5 h / Heating
7: 18 percent / ethanol / 0.08 h / 0 °C / Irradiation
With pyridine; 2,4,6-trimethyl-pyridine; dmap; N-Bromosuccinimide; lithium aluminium tetrahydride; n-butyllithium; water; sodium hydrogencarbonate; methyl iodide; In tetrahydrofuran; ethanol; acetone;
DOI:10.1248/cpb.40.648
Guidance literature:
Multi-step reaction with 5 steps
1: 1.) n-BuLi / 1.) THF, n-hexane, 4 deg C, 2 h, 2.) THF, n-hexane, 4 deg C, 1 h
2: 83 percent / CH3I, H2O / acetone / 20 h / Heating
3: 60 percent / tetrahydrofuran / 0.5 h / Ambient temperature
4: 86 percent / 4-dimethylaminopyridine, pyridine / 49 h / Ambient temperature
5: 1.) NBS, NaHCO3, 2.) γ-collidine
With pyridine; 2,4,6-trimethyl-pyridine; dmap; N-Bromosuccinimide; n-butyllithium; water; sodium hydrogencarbonate; methyl iodide; In tetrahydrofuran; acetone;
DOI:10.1248/cpb.40.648
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