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8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)-

Base Information
  • Chemical Name:8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)-
  • CAS No.:173443-27-1
  • Molecular Formula:C22H29NO6
  • Molecular Weight:403.475
  • Hs Code.:
8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-,
5-carboxypentyl ester, (1R,2R,3S,5S)-

Synonyms:

Suppliers and Price of 8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)-
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)-
Chemical Property:
  • PSA:93.14000 
  • LogP:2.82080 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)-

There total 7 articles about 8-Azabicyclo[3.2.1]octane-2-carboxylic acid, 3-(benzoyloxy)-8-methyl-, 5-carboxypentyl ester, (1R,2R,3S,5S)- 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 4 steps
1: 100 percent / aq. hydrochloride / 22 h / Heating
2: 48 percent / Me4NOH*5H2O; Et4NI / dimethylformamide; tetrahydrofuran / 20 h / 60 °C
3: 82 percent / Et3N / toluene / 3 h / Heating
4: 90 percent / H2 / Pd/C / ethyl acetate; ethanol / 0.5 h / 20 °C
With hydrogenchloride; tetramethyl ammoniumhydroxide; tetraethylammonium iodide; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ja043935e
Guidance literature:
Multi-step reaction with 3 steps
1: 48 percent / Me4NOH*5H2O; Et4NI / dimethylformamide; tetrahydrofuran / 20 h / 60 °C
2: 82 percent / Et3N / toluene / 3 h / Heating
3: 90 percent / H2 / Pd/C / ethyl acetate; ethanol / 0.5 h / 20 °C
With tetramethyl ammoniumhydroxide; tetraethylammonium iodide; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/ja043935e
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