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2-Boc-8-oxo-2-azaspiro[4.5]decane

Base Information Edit
  • Chemical Name:2-Boc-8-oxo-2-azaspiro[4.5]decane
  • CAS No.:1272758-17-4
  • Molecular Formula:C14H23NO3
  • Molecular Weight:253.342
  • Hs Code.:
  • Mol file:1272758-17-4.mol
2-Boc-8-oxo-2-azaspiro[4.5]decane

Synonyms:

Suppliers and Price of 2-Boc-8-oxo-2-azaspiro[4.5]decane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • tert-butyl8-oxo-2-azaspiro[4.5]decane-2-carboxylate
  • 50mg
  • $ 220.00
  • Synthonix
  • 2-Boc-8-oxo-2-azaspiro[4.5]decane 97.0%
  • 250mg
  • $ 260.00
  • SynQuest Laboratories
  • tert-Butyl 8-oxo-2-azaspiro[4.5]decane-2-carboxylate 97.0%
  • 250 mg
  • $ 928.00
  • Matrix Scientific
  • 2-Boc-8-oxo-2-azaspiro[4.5]decane 97.0%
  • 1g
  • $ 2112.00
  • Chemenu
  • tert-butyl8-oxo-2-azaspiro[4.5]decane-2-carboxylate 97%
  • 1g
  • $ 748.00
  • Chemenu
  • tert-butyl8-oxo-2-azaspiro[4.5]decane-2-carboxylate 97%
  • 250mg
  • $ 253.00
  • AstaTech
  • 2-BOC-8-OXO-2-AZASPIRO[4.5]DECANE 97%
  • 0.25 / G
  • $ 329.00
  • AstaTech
  • 2-BOC-8-OXO-2-AZASPIRO[4.5]DECANE 97%
  • 0.1 / G
  • $ 299.00
  • AstaTech
  • 2-BOC-8-OXO-2-AZASPIRO[4.5]DECANE 97%
  • 1 / G
  • $ 519.00
  • American Custom Chemicals Corporation
  • TERT-BUTYL-8-OXO-2-AZASPIRO[4.5]DECANE-2-CARBOXYLATE 95.00%
  • 5MG
  • $ 454.60
Total 10 raw suppliers
Chemical Property of 2-Boc-8-oxo-2-azaspiro[4.5]decane Edit
Chemical Property:
  • Storage Temp.:Sealed in dry,Room Temperature 
Purity/Quality:

97% *data from raw suppliers

tert-butyl8-oxo-2-azaspiro[4.5]decane-2-carboxylate *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-Boc-8-oxo-2-azaspiro[4.5]decane

There total 11 articles about 2-Boc-8-oxo-2-azaspiro[4.5]decane 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:
With pyridinium p-toluenesulfonate; In tetrahydrofuran; water; at 70 ℃; for 15h;
Guidance literature:
With sodium carbonate; In tetrahydrofuran; water; at 20 ℃; for 2h;
Guidance literature:
Multi-step reaction with 5 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 h / Reflux
2: hydrogen / water; ethanol / 72 h / 20 °C
3: lithium aluminium tetrahydride / tetrahydrofuran / 3 h / 0 °C / Inert atmosphere; Reflux
4: hydrogenchloride / water; methanol / 20 °C
5: sodium carbonate / water; tetrahydrofuran / 2 h / 20 °C
With hydrogenchloride; lithium aluminium tetrahydride; tetrabutyl ammonium fluoride; hydrogen; sodium carbonate; In tetrahydrofuran; methanol; ethanol; water;
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