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5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose

Base Information
  • Chemical Name:5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose
  • CAS No.:108788-63-2
  • Molecular Formula:C18H23NO7
  • Molecular Weight:365.383
  • Hs Code.:
5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose

Synonyms:5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose

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Chemical Property of 5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose
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Technology Process of 5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose

There total 8 articles about 5,7-anhydro-6-N-benzyloxycarbonylamino-6-deoxy-1,2-O-isopropylidene-α-D-glycero-L-ido-heptofuranose 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 7 steps
1: 88 percent / diisobutylaluminium hydride / hexane; toluene / 3 h / Ambient temperature
2: 52 percent / m-chloroperbezoic acid / CH2Cl2 / 16 h / Ambient temperature
3: 88 percent / sodium azide; ammonium chloride / H2O; 2-methoxy-ethanol / 2 h / 125 °C
4: 70 percent / pyridine / 10 h
5: 77 percent / potassium tert-butoxide / benzene; tetrahydrofuran / 0.33 h / 0 °C
6: H2 / 10 percent Pd-C / acetic acid; tetrahydrofuran; H2O
7: sodium carbonate / methanol; H2O / 5 h / 0 °C
With pyridine; sodium azide; ammonium chloride; potassium tert-butylate; hydrogen; diisobutylaluminium hydride; sodium carbonate; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; hexane; dichloromethane; 2-methoxy-ethanol; water; acetic acid; toluene; benzene;
DOI:10.1248/cpb.34.3102
Guidance literature:
Multi-step reaction with 8 steps
1: 55 percent / benzene / 38 h / Ambient temperature
2: 88 percent / diisobutylaluminium hydride / hexane; toluene / 3 h / Ambient temperature
3: 52 percent / m-chloroperbezoic acid / CH2Cl2 / 16 h / Ambient temperature
4: 88 percent / sodium azide; ammonium chloride / H2O; 2-methoxy-ethanol / 2 h / 125 °C
5: 70 percent / pyridine / 10 h
6: 77 percent / potassium tert-butoxide / benzene; tetrahydrofuran / 0.33 h / 0 °C
7: H2 / 10 percent Pd-C / acetic acid; tetrahydrofuran; H2O
8: sodium carbonate / methanol; H2O / 5 h / 0 °C
With pyridine; sodium azide; ammonium chloride; potassium tert-butylate; hydrogen; diisobutylaluminium hydride; sodium carbonate; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; hexane; dichloromethane; 2-methoxy-ethanol; water; acetic acid; toluene; benzene;
DOI:10.1248/cpb.34.3102
Guidance literature:
Multi-step reaction with 6 steps
1: 52 percent / m-chloroperbezoic acid / CH2Cl2 / 16 h / Ambient temperature
2: 88 percent / sodium azide; ammonium chloride / H2O; 2-methoxy-ethanol / 2 h / 125 °C
3: 70 percent / pyridine / 10 h
4: 77 percent / potassium tert-butoxide / benzene; tetrahydrofuran / 0.33 h / 0 °C
5: H2 / 10 percent Pd-C / acetic acid; tetrahydrofuran; H2O
6: sodium carbonate / methanol; H2O / 5 h / 0 °C
With pyridine; sodium azide; ammonium chloride; potassium tert-butylate; hydrogen; sodium carbonate; 3-chloro-benzenecarboperoxoic acid; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; 2-methoxy-ethanol; water; acetic acid; benzene;
DOI:10.1248/cpb.34.3102
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