Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate

Base Information Edit
  • Chemical Name:(1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate
  • CAS No.:111646-96-9
  • Molecular Formula:C18H26N2O3
  • Molecular Weight:318.416
  • Hs Code.:
  • Mol file:111646-96-9.mol
(1R,2R,2'S,4E)-1-(N<sub>1</sub>,N<sub>2</sub>-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate

Synonyms:(1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate

Suppliers and Price of (1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate
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 0 raw suppliers
Chemical Property of (1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate

There total 5 articles about (1R,2R,2'S,4E)-1-(N1,N2-dimethylglycinamide-2'-yl)-2-methyl-4-hexenyl benzoate 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 3 steps
1: 82 percent / (i-Pr)2NH, BuLi / tetrahydrofuran; hexane / 1.) -75 degC, 20 min; 2.) -100 degC, 50 min; 3.) 30 min, r.t.
2: 84 percent / 40 percent aq. NaOH / acetone / 12 h / 50 °C
3: 100 percent / 2 N HCl / ethanol / 4 h / 90 °C
With hydrogenchloride; sodium hydroxide; n-butyllithium; diisopropylamine; In tetrahydrofuran; ethanol; hexane; acetone;
DOI:10.1002/hlca.19870700129
Guidance literature:
Multi-step reaction with 4 steps
2: 82 percent / (i-Pr)2NH, BuLi / tetrahydrofuran; hexane / 1.) -75 degC, 20 min; 2.) -100 degC, 50 min; 3.) 30 min, r.t.
3: 84 percent / 40 percent aq. NaOH / acetone / 12 h / 50 °C
4: 100 percent / 2 N HCl / ethanol / 4 h / 90 °C
With hydrogenchloride; sodium hydroxide; n-butyllithium; diisopropylamine; In tetrahydrofuran; ethanol; hexane; acetone;
DOI:10.1002/hlca.19870700129
Post RFQ for Price