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methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate

Base Information
  • Chemical Name:methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate
  • CAS No.:122849-84-7
  • Molecular Formula:C35H42O9
  • Molecular Weight:606.713
  • Hs Code.:
methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate

Synonyms:

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Chemical Property of methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate
Chemical Property:
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Technology Process of methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate

There total 21 articles about methyl 3-<5-benzyloxy-2-methoxycarbonyl-3-(3-oxopentyl)phenoxy>-4,6-dimethoxy-2-pentylbenzoate 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 15 steps
1: 95 percent / thionyl chloride, pyridine / CH2Cl2 / 3 h / Ambient temperature
2: 88 percent / dimethylformamide / 7 h / Ambient temperature
3: 91 percent / 30percent aq. sodium hydroxide / methanol / 72 h / Heating
4: 95 percent / potassium carbonate / acetone / 3 h / Heating
5: 95 percent / lithium aluminium hydride / diethyl ether / 2 h / Heating
6: 85 percent / pyridine / CHCl3 / 3 h / 0 °C
7: 94 percent / 1,2-dimethoxyethane / dimethylsulfoxide / 18 h / Ambient temperature
8: 81 percent / ether / benzene / 1 h / Ambient temperature; aq. hydrochloric acid, ethyl acetate, 16 h
9: 98 percent / trifluoroacetic anhydride, / nitromethane / 1.5 h / 0 °C
10: 81 percent / H2, conc. hydrochloric acid (4 drops) / 10percent palladized charcoal / ethyl acetate
11: 73 percent / potassium cyanoferrate(III), potassium carbonate / H2O; dioxane / 0.17 h
12: 70 percent / various solvent(s) / 0.17 h / Heating
13: 94 percent / potassium carbonate / dimethylformamide / Ambient temperature
14: 66 percent / sodium methoxide / methanol / 3 h / Ambient temperature
15: 82 percent / potassium carbonate / dimethylformamide / 5 h / Ambient temperature
With pyridine; hydrogenchloride; sodium hydroxide; lithium aluminium tetrahydride; 1,2-dimethoxyethane; thionyl chloride; diethyl ether; hydrogen; sodium methylate; potassium carbonate; trifluoroacetic anhydride; potassium hexacyanoferrate(III); palladium on activated charcoal; In 1,4-dioxane; methanol; diethyl ether; nitromethane; dichloromethane; chloroform; water; dimethyl sulfoxide; ethyl acetate; N,N-dimethyl-formamide; acetone; benzene;
Guidance literature:
Multi-step reaction with 11 steps
1: 77 percent / potassium carbonate / acetone / 24 h / Heating
2: 89 percent / potassium carbonate / acetone / Heating
3: 80 percent / phosphoryl chloride / 24 h / 70 °C
4: 97 percent / sodium chlorite, sulphamic acid / H2O; dioxane / 0.67 h
5: 98 percent / trifluoroacetic anhydride, / nitromethane / 1.5 h / 0 °C
6: 81 percent / H2, conc. hydrochloric acid (4 drops) / 10percent palladized charcoal / ethyl acetate
7: 73 percent / potassium cyanoferrate(III), potassium carbonate / H2O; dioxane / 0.17 h
8: 70 percent / various solvent(s) / 0.17 h / Heating
9: 94 percent / potassium carbonate / dimethylformamide / Ambient temperature
10: 66 percent / sodium methoxide / methanol / 3 h / Ambient temperature
11: 82 percent / potassium carbonate / dimethylformamide / 5 h / Ambient temperature
With hydrogenchloride; sodium chlorite; aminosulfonic acid; hydrogen; sodium methylate; potassium carbonate; trifluoroacetic anhydride; potassium hexacyanoferrate(III); trichlorophosphate; palladium on activated charcoal; In 1,4-dioxane; methanol; nitromethane; water; ethyl acetate; N,N-dimethyl-formamide; acetone;
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