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1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-

Base Information
  • Chemical Name:1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-
  • CAS No.:169822-66-6
  • Molecular Formula:C12H20O4
  • Molecular Weight:228.288
  • Hs Code.:
  • Mol file:169822-66-6.mol
1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-

Synonyms:1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid,3,3-dimethyl;

Suppliers and Price of 1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 5 raw suppliers
Chemical Property of 1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-
Chemical Property:
  • PSA:55.76000 
  • LogP:2.03050 
Purity/Quality:

99.3% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
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Technology Process of 1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl-

There total 1 articles about 1,5-Dioxaspiro[5.5]undecane-9-carboxylic acid, 3,3-dimethyl- 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 sodium hydroxide; In methanol;
DOI:10.1021/jp0271716
Guidance literature:
3,3-Dimethyl-1,5-dioxaspiro[5.5]undecane-9-carboxylic acid; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at 50 ℃; for 2h;
9-(1-Phenylpiperidin-4-ylidene)cyclohexanone; In tetrahydrofuran; hexane; at 50 ℃; for 2h;
DOI:10.1021/jp0271716
Guidance literature:
3,3-Dimethyl-1,5-dioxaspiro[5.5]undecane-9-carboxylic acid; With lithium diisopropyl amide; In tetrahydrofuran; hexane; at 50 ℃; for 2h; Further stages.;
DOI:10.1021/ja983716r
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