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25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester

Base Information
  • Chemical Name:25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester
  • CAS No.:80097-58-1
  • Molecular Formula:C25H34O3
  • Molecular Weight:382.543
  • Hs Code.:
25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester

Synonyms:25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester

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Chemical Property of 25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester
Chemical Property:
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Technology Process of 25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester

There total 1 articles about 25,26,27-trisnorcholesta-1,4,6-trien-3-on-24-oic acid methyl ester 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: 76 percent / POCl3, pyridine / 16 h / Ambient temperature
2: 98 percent / tri-N-methylanilinium perbromide / tetrahydrofuran / 1.) 0 deg C, 15 min, 2.) r.t., 30 min
3: Li2CO3, LiBr / dimethylformamide / 0.5 h / Heating
With pyridine; phenyltrimethylammonium tribromide; lithium carbonate; lithium bromide; trichlorophosphate; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)86327-4
Guidance literature:
Multi-step reaction with 14 steps
1: 80 percent / 5percent NaOH, 30percent H2O2 / methanol / 18 h / Heating
2: 65 percent / lithium, anhydrous NH4Cl / liquid ammonia; tetrahydrofuran / 2 h / -78 °C
4: 149 mg / pyridine / 0 °C
5: 53 percent / LiBr / dimethylformamide / 2 h / Heating
6: 92 percent / dimethylformamide / 4 h / 70 - 80 °C
7: 85 percent / 5percent KOH / methanol; tetrahydrofuran / 18 h / Ambient temperature
8: 57 percent / triethylamine / pyridine / 15 h / Ambient temperature
9: 74 percent / diisopropylamine, n-BuLi / tetrahydrofuran / 0.05 h / -78 °C
10: 99 percent / 1N HCl / 1,2-dimethoxy-ethane; methanol / 1 h / Ambient temperature
11: 72 percent / Na2HPO4, 5percent Na(Hg) / methanol / 2.25 h / Ambient temperature
12: 98 percent / 4-dimethylaminopyridine / pyridine / 20 h / Ambient temperature
14: 1.) benzene, ethanol, ice-cooling, irradiation, 2.5 min; 2.) benzene, ethanol, reflux, 1 h
With hydrogenchloride; potassium hydroxide; sodium hydroxide; disodium hydrogenphosphate; n-butyllithium; sodium amalgam; dihydrogen peroxide; lithium; ammonium chloride; triethylamine; diisopropylamine; lithium bromide; dmap; In tetrahydrofuran; pyridine; methanol; 1,2-dimethoxyethane; ammonia; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.4297
Guidance literature:
Multi-step reaction with 9 steps
1: 80 percent / 5percent NaOH, 30percent H2O2 / methanol / 18 h / Heating
2: 65 percent / lithium, anhydrous NH4Cl / liquid ammonia; tetrahydrofuran / 2 h / -78 °C
4: 149 mg / pyridine / 0 °C
5: 53 percent / LiBr / dimethylformamide / 2 h / Heating
6: 92 percent / dimethylformamide / 4 h / 70 - 80 °C
7: 85 percent / 5percent KOH / methanol; tetrahydrofuran / 18 h / Ambient temperature
8: 57 percent / triethylamine / pyridine / 15 h / Ambient temperature
9: 74 percent / diisopropylamine, n-BuLi / tetrahydrofuran / 0.05 h / -78 °C
With potassium hydroxide; sodium hydroxide; n-butyllithium; dihydrogen peroxide; lithium; ammonium chloride; triethylamine; diisopropylamine; lithium bromide; In tetrahydrofuran; pyridine; methanol; ammonia; N,N-dimethyl-formamide;
DOI:10.1248/cpb.30.4297
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