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methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate

Base Information
  • Chemical Name:methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate
  • CAS No.:101696-59-7
  • Molecular Formula:C23H30O13S
  • Molecular Weight:546.549
  • Hs Code.:
methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate

Synonyms:methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate

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Chemical Property of methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate
Chemical Property:
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Technology Process of methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate

There total 13 articles about methyl 6-deoxy-5-O-(phenylmethyl)-L-glycero-β-D-allo-octofuranuronate 1,2,3-triacetate 7-methanesulfonate 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 13 steps
1: 1.) zinc chloride, 2.) trifluoroacetic acid / 1.) THF, r.t., 9 h, 2.) r.t., 3 h
2: 11.5 g / CeCl3*7H2O, NaBH4 / methanol / 1 h / -78 °C
3: 13.5 g / 50 percent NaH / dimethylformamide; paraffin / 0 °C
4: 1.) NaIO4, OsO4, 2.) 5 percent aq. K2CO3 / 1.) dioxane/H2O, r.t., overnight, 2.) MeOH, r.t., 1 h
5: 86 percent / Ag2CO3-Celite / xylene / 1.5 h / Heating
6: lithium hydroxide monohydrate, H2O / 1,2-dimethoxy-ethane / 2 h / 50 °C
7: 1.) 50 percent NaH, 2.) 1 N HCl / dimethylformamide; paraffin
8: diethyl ether; methanol
9: 62 percent / DDQ, H2O / CH2Cl2 / 24 h
10: 83 percent / triethylamine / CH2Cl2 / 1.) -20 deg C, 3 h, 2.) 0 deg C, 3 h
11: 1 N HCl / methanol / 1.5 h / Heating
12: 248 mg / pyridine / 5 h
13: 152 mg / acetic acid, conc. H2SO4 / CH2Cl2 / 1 h / 0 °C
With pyridine; hydrogenchloride; lithium hydroxide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; cerium(III) chloride; sulfuric acid; water; sodium hydride; potassium carbonate; acetic acid; triethylamine; silver carbonate; trifluoroacetic acid; 2,3-dicyano-5,6-dichloro-p-benzoquinone; zinc(II) chloride; In methanol; 1,2-dimethoxyethane; diethyl ether; dichloromethane; N,N-dimethyl-formamide; paraffin; xylene;
DOI:10.1021/ja00230a024
Guidance literature:
Multi-step reaction with 12 steps
1: 11.5 g / CeCl3*7H2O, NaBH4 / methanol / 1 h / -78 °C
2: 13.5 g / 50 percent NaH / dimethylformamide; paraffin / 0 °C
3: 1.) NaIO4, OsO4, 2.) 5 percent aq. K2CO3 / 1.) dioxane/H2O, r.t., overnight, 2.) MeOH, r.t., 1 h
4: 86 percent / Ag2CO3-Celite / xylene / 1.5 h / Heating
5: lithium hydroxide monohydrate, H2O / 1,2-dimethoxy-ethane / 2 h / 50 °C
6: 1.) 50 percent NaH, 2.) 1 N HCl / dimethylformamide; paraffin
7: diethyl ether; methanol
8: 62 percent / DDQ, H2O / CH2Cl2 / 24 h
9: 83 percent / triethylamine / CH2Cl2 / 1.) -20 deg C, 3 h, 2.) 0 deg C, 3 h
10: 1 N HCl / methanol / 1.5 h / Heating
11: 248 mg / pyridine / 5 h
12: 152 mg / acetic acid, conc. H2SO4 / CH2Cl2 / 1 h / 0 °C
With pyridine; hydrogenchloride; lithium hydroxide; sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; cerium(III) chloride; sulfuric acid; water; sodium hydride; potassium carbonate; acetic acid; triethylamine; silver carbonate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In methanol; 1,2-dimethoxyethane; diethyl ether; dichloromethane; N,N-dimethyl-formamide; paraffin; xylene;
DOI:10.1021/ja00230a024
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