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(+/-)-anisomycin

Base Information
  • Chemical Name:(+/-)-anisomycin
  • CAS No.:21497-40-5
  • Molecular Formula:C14H19NO4
  • Molecular Weight:265.309
  • Hs Code.:
(+/-)-anisomycin

Synonyms:(+/-)-anisomycin

Suppliers and Price of (+/-)-anisomycin
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (+/-)-anisomycin
Chemical Property:
Purity/Quality:

98%,99%, *data from raw suppliers

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Technology Process of (+/-)-anisomycin

There total 11 articles about (+/-)-anisomycin 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 9 steps
1: 67 percent / zinc dust, aq. HCl / ethanol / 1.) 1.5 h, 2.) reflux, 1.5 h
2: 94 percent / aq. NaOH / toluene / 1 h / 3 - 5 °C
3: 82 percent / N-iodosuccinimide, aq. perchloric acid / tetrahydrofuran / 1.) 3-5 deg C, 1 h, 2.) 3-5 deg C -> room temperature, 1 h
4: 92 percent / 5percent KOH, EtOH / 0.5 h
5: 100 percent / hydrogen / 10percent Pd/C / methanol / 2 h
6: trifluoroacetic acid, sodium trifluoroacetate / 16 h / Heating
7: aq. Na2CO3 / tetrahydrofuran / 1 h / 3 - 5 °C / pH 9
8: 1.) pyridine, 2.) pyridine / 1.) CH2Cl2, 3-5 deg C, 30 min, 2.) 18 h
9: 1.) zinc powder, acetic acid, 2.) hydrogen / 2.) 10percent Pd/C / 1.) THF, 1 h, 2.) MeOH, 2 h
With pyridine; hydrogenchloride; potassium hydroxide; sodium hydroxide; N-iodo-succinimide; perchloric acid; ethanol; hydrogen; sodium 2,2,2-trifluoroacetate; sodium carbonate; acetic acid; trifluoroacetic acid; zinc; palladium on activated charcoal; In tetrahydrofuran; methanol; ethanol; toluene;
DOI:10.1021/ja00386a039
Guidance literature:
Multi-step reaction with 8 steps
1: 94 percent / aq. NaOH / toluene / 1 h / 3 - 5 °C
2: 82 percent / N-iodosuccinimide, aq. perchloric acid / tetrahydrofuran / 1.) 3-5 deg C, 1 h, 2.) 3-5 deg C -> room temperature, 1 h
3: 92 percent / 5percent KOH, EtOH / 0.5 h
4: 100 percent / hydrogen / 10percent Pd/C / methanol / 2 h
5: trifluoroacetic acid, sodium trifluoroacetate / 16 h / Heating
6: aq. Na2CO3 / tetrahydrofuran / 1 h / 3 - 5 °C / pH 9
7: 1.) pyridine, 2.) pyridine / 1.) CH2Cl2, 3-5 deg C, 30 min, 2.) 18 h
8: 1.) zinc powder, acetic acid, 2.) hydrogen / 2.) 10percent Pd/C / 1.) THF, 1 h, 2.) MeOH, 2 h
With pyridine; potassium hydroxide; sodium hydroxide; N-iodo-succinimide; perchloric acid; ethanol; hydrogen; sodium 2,2,2-trifluoroacetate; sodium carbonate; acetic acid; trifluoroacetic acid; zinc; palladium on activated charcoal; In tetrahydrofuran; methanol; toluene;
DOI:10.1021/ja00386a039
Guidance literature:
Multi-step reaction with 7 steps
1: 82 percent / N-iodosuccinimide, aq. perchloric acid / tetrahydrofuran / 1.) 3-5 deg C, 1 h, 2.) 3-5 deg C -> room temperature, 1 h
2: 92 percent / 5percent KOH, EtOH / 0.5 h
3: 100 percent / hydrogen / 10percent Pd/C / methanol / 2 h
4: trifluoroacetic acid, sodium trifluoroacetate / 16 h / Heating
5: aq. Na2CO3 / tetrahydrofuran / 1 h / 3 - 5 °C / pH 9
6: 1.) pyridine, 2.) pyridine / 1.) CH2Cl2, 3-5 deg C, 30 min, 2.) 18 h
7: 1.) zinc powder, acetic acid, 2.) hydrogen / 2.) 10percent Pd/C / 1.) THF, 1 h, 2.) MeOH, 2 h
With pyridine; potassium hydroxide; N-iodo-succinimide; perchloric acid; ethanol; hydrogen; sodium 2,2,2-trifluoroacetate; sodium carbonate; acetic acid; trifluoroacetic acid; zinc; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1021/ja00386a039
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