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2-oxa-7-azaspiro[3.5]nonane acetate

Base Information Edit
  • Chemical Name:2-oxa-7-azaspiro[3.5]nonane acetate
  • CAS No.:1313369-52-6
  • Molecular Formula:C2H4O2*C7H13NO
  • Molecular Weight:187.239
  • Hs Code.:
  • Mol file:1313369-52-6.mol
2-oxa-7-azaspiro[3.5]nonane acetate

Synonyms:

Suppliers and Price of 2-oxa-7-azaspiro[3.5]nonane acetate
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
  • 2-Oxa-7-aza-spiro[3.5]nonaneaceticacidsalt
  • 100mg
  • $ 330.00
  • J&W Pharmlab
  • 2-Oxa-7-aza-spiro[3.5]nonaneaceticacidsalt 97%
  • 1g
  • $ 498.00
  • Crysdot
  • 2-Oxa-7-azaspiro[3.5]nonaneacetate 95+%
  • 1g
  • $ 880.00
  • Chemenu
  • 2-oxa-7-azaspiro[3.5]nonaneacetate 95%
  • 1g
  • $ 830.00
  • Alichem
  • 2-Oxa-7-azaspiro[3.5]nonaneacetate
  • 1g
  • $ 706.86
Total 4 raw suppliers
Chemical Property of 2-oxa-7-azaspiro[3.5]nonane acetate Edit
Chemical Property:
Purity/Quality:

97% *data from raw suppliers

2-Oxa-7-aza-spiro[3.5]nonaneaceticacidsalt *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-oxa-7-azaspiro[3.5]nonane acetate

There total 5 articles about 2-oxa-7-azaspiro[3.5]nonane acetate 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 2 steps
1: palladium 10% on activated carbon; hydrogen / methanol / 20 °C
2: dichloromethane / 0.25 h / 0 °C
With palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane;
DOI:10.1016/j.tetlet.2011.04.054
Guidance literature:
Multi-step reaction with 5 steps
1.1: lithium borohydride / tetrahydrofuran; toluene / 60 °C
2.1: n-butyllithium / tetrahydrofuran / 0.5 h / 0 °C
2.2: 1.5 h / 0 °C
2.3: 1.5 h / 0 - 60 °C
3.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C
3.2: 2 h / 20 °C
4.1: palladium 10% on activated carbon; hydrogen / methanol / 20 °C
5.1: dichloromethane / 0.25 h / 0 °C
With lithium borohydride; n-butyllithium; palladium 10% on activated carbon; hydrogen; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; toluene;
DOI:10.1016/j.tetlet.2011.04.054
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