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C11H17NO4

Base Information
  • Chemical Name:C11H17NO4
  • CAS No.:1453315-97-3
  • Molecular Formula:C11H17NO4
  • Molecular Weight:227.26
  • Hs Code.:
C<sub>11</sub>H<sub>17</sub>NO<sub>4</sub>

Synonyms:

Suppliers and Price of C11H17NO4
Supply Marketing:
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
  • Sigma-Aldrich
  • 2-Boc-8-oxo-5-oxa-2-azaspiro[3.4]octane 95%
  • 100mg
  • $ 446.00
  • Crysdot
  • tert-Butyl8-oxo-5-oxa-2-azaspiro[3.4]octane-2-carboxylate 95%
  • 5g
  • $ 3572.00
  • Crysdot
  • tert-Butyl8-oxo-5-oxa-2-azaspiro[3.4]octane-2-carboxylate 95%
  • 1g
  • $ 1191.00
  • Chemenu
  • tert-Butyl8-oxo-5-oxa-2-azaspiro[3.4]octane-2-carboxylate 95%
  • 1g
  • $ 1122.00
  • American Custom Chemicals Corporation
  • TERT-BUTYL-8-OXO-5-OXA-2-AZASPIRO[3.4]OCTANE-2-CARBOXYLATE 95.00%
  • 5MG
  • $ 455.23
  • AK Scientific
  • 2-Boc-8-oxo-5-oxa-2-azaspiro[3.4]octane
  • 100mg
  • $ 613.00
Total 5 raw suppliers
Chemical Property of C11H17NO4
Chemical Property:
  • Melting Point:63-68°C 
Purity/Quality:

99%, *data from raw suppliers

2-Boc-8-oxo-5-oxa-2-azaspiro[3.4]octane 95% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of C11H17NO4

There total 3 articles about C11H17NO4 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 toluene-4-sulfonic acid; In acetone; at 0 - 20 ℃; for 0.833333h; Inert atmosphere;
DOI:10.1021/ol402127b
Guidance literature:
Multi-step reaction with 3 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere
1.2: 3 h / -78 °C / Inert atmosphere
2.1: potassium tert-butylate; perhydrodibenzo-18-crown-6 / tert-butyl alcohol / 9 h / Inert atmosphere; Reflux
3.1: toluene-4-sulfonic acid / acetone / 0.83 h / 0 - 20 °C / Inert atmosphere
With perhydrodibenzo-18-crown-6; n-butyllithium; potassium tert-butylate; toluene-4-sulfonic acid; In tetrahydrofuran; hexane; acetone; tert-butyl alcohol;
DOI:10.1021/ol402127b
Guidance literature:
Multi-step reaction with 2 steps
1: potassium tert-butylate; perhydrodibenzo-18-crown-6 / tert-butyl alcohol / 9 h / Inert atmosphere; Reflux
2: toluene-4-sulfonic acid / acetone / 0.83 h / 0 - 20 °C / Inert atmosphere
With perhydrodibenzo-18-crown-6; potassium tert-butylate; toluene-4-sulfonic acid; In acetone; tert-butyl alcohol;
DOI:10.1021/ol402127b
upstream raw materials:

tert-butyl 3-oxoazetidine-1-carboxylate

C12H19NO4

C12H19NO4

Downstream raw materials:

C11H19NO4

C11H20N2O3

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