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2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol

Base Information
  • Chemical Name:2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol
  • CAS No.:129286-04-0
  • Molecular Formula:C19H26O3
  • Molecular Weight:302.414
  • Hs Code.:
2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol

Synonyms:2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol

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Chemical Property of 2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol
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Technology Process of 2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol

There total 10 articles about 2-O-benzyl-<8-methyl-2,3,4,4a,8,9-hexahydro-(4aS,6Z,8S,9aR)-pyrano<3,2-b>oxepan-6-yl>ethanol 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: 95 percent / H2 / 10percent Pd/C / 0.5 h
2: 61 percent / Lawesson's reagent / toluene / 12 h / Heating
With Lawessons reagent; hydrogen; palladium on activated charcoal; In toluene;
DOI:10.1021/ja00173a013
Guidance literature:
Multi-step reaction with 8 steps
1: 88 percent / ZnBr2 / diethyl ether / 0.33 h / -78 °C
2: 100 percent / H2 / Pd(OH)2 / methanol / 3 h / 25 °C
3: 1.) Ph3P, dipyridyl disulfide, 2.) AgClO4 / 1.) THF, 25 deg C, 30 min, 2.) benzene, 80 deg C, 1 h
4: HF*pyridine / tetrahydrofuran / 2 h / Ambient temperature
5: NEt3, methanesulfonyl chloride, DBU / benzene; CH2Cl2 / 1 h / 45 °C
6: 95 percent / H2 / 10percent Pd/C / 0.5 h
7: 61 percent / Lawesson's reagent / toluene / 12 h / Heating
With Lawessons reagent; 2,2'-dipyridyldisulphide; hydrogen; silver perchlorate; pyridine hydrogenfluoride; methanesulfonyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine; zinc dibromide; palladium dihydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; benzene;
DOI:10.1021/ja00173a013
Guidance literature:
Multi-step reaction with 9 steps
1: oxalyl chloride, DMSO / CH2Cl2 / 0.75 h / -78 °C
2: 88 percent / ZnBr2 / diethyl ether / 0.33 h / -78 °C
3: 100 percent / H2 / Pd(OH)2 / methanol / 3 h / 25 °C
4: 1.) Ph3P, dipyridyl disulfide, 2.) AgClO4 / 1.) THF, 25 deg C, 30 min, 2.) benzene, 80 deg C, 1 h
5: HF*pyridine / tetrahydrofuran / 2 h / Ambient temperature
6: NEt3, methanesulfonyl chloride, DBU / benzene; CH2Cl2 / 1 h / 45 °C
7: 95 percent / H2 / 10percent Pd/C / 0.5 h
8: 61 percent / Lawesson's reagent / toluene / 12 h / Heating
With Lawessons reagent; oxalyl dichloride; 2,2'-dipyridyldisulphide; hydrogen; silver perchlorate; pyridine hydrogenfluoride; dimethyl sulfoxide; methanesulfonyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; triphenylphosphine; zinc dibromide; palladium dihydroxide; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; toluene; benzene;
DOI:10.1021/ja00173a013
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