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4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene

Base Information Edit
  • Chemical Name:4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene
  • CAS No.:38970-57-9
  • Molecular Formula:C15H24O
  • Molecular Weight:0
  • Hs Code.:2932999099
  • Mol file:38970-57-9.mol
4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene

Synonyms:Bisabolenoxid;1-Oxaspiro(4.5)dec-7-ene,4,8-dimethyl-2-(2-methyl-1-propenyl);4,8-dimethyl-2-(2-methyl-propenyl)-1-oxa-spiro[4.5]dec-7-ene;bisabolene oxide;4,8-dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro(4.5)dec-7-ene;

Suppliers and Price of 4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene
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
Total 3 raw suppliers
Chemical Property of 4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene Edit
Chemical Property:
  • PSA:9.23000 
  • LogP:4.24660 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene

There total 6 articles about 4,8-Dimethyl-2-(2-methyl-1-propenyl)-1-oxaspiro[4.5]dec-7-ene 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 p-toluenesulfonyl chloride; In pyridine; at 0 - 25 ℃; for 24h;
DOI:10.1016/S0040-4020(01)91487-5
Guidance literature:
Multi-step reaction with 6 steps
1: 1.) Mg, I2 / 1.) THF, 15 grad C, 2 h; 2.) heating, 1 h
2: 1.) BH3; 2.) 2 N NaOH, 30 percent H2O2, K2CO3 / 1.) THF, 0 grad C, 3 h; 2.) 1 h
3: 59 percent / pyridinium chlorochromate / CH2Cl2 / 2 h
4: 1.) 20 percent DIBAH; 2.) ice, acetic acid / 1.) toluene, -78 grad C, 3 h; 2.) 0 grad C
5: 1.) Mg, I2 / 1.) THF, 75 grad C, 1 h; 2.) THF, heating, 24 h
6: 39 percent / tosyl chloride / pyridine / 24 h / 0 - 25 °C
With sodium hydroxide; Methamphetamin; borane; dihydrogen peroxide; iodine; diisobutylaluminium hydride; potassium carbonate; magnesium; acetic acid; p-toluenesulfonyl chloride; pyridinium chlorochromate; In pyridine; dichloromethane;
DOI:10.1016/S0040-4020(01)91487-5
Guidance literature:
Multi-step reaction with 4 steps
1: 59 percent / pyridinium chlorochromate / CH2Cl2 / 2 h
2: 1.) 20 percent DIBAH; 2.) ice, acetic acid / 1.) toluene, -78 grad C, 3 h; 2.) 0 grad C
3: 1.) Mg, I2 / 1.) THF, 75 grad C, 1 h; 2.) THF, heating, 24 h
4: 39 percent / tosyl chloride / pyridine / 24 h / 0 - 25 °C
With Methamphetamin; iodine; diisobutylaluminium hydride; magnesium; acetic acid; p-toluenesulfonyl chloride; pyridinium chlorochromate; In pyridine; dichloromethane;
DOI:10.1016/S0040-4020(01)91487-5
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