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(3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate

Base Information
  • Chemical Name:(3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate
  • CAS No.:870640-64-5
  • Molecular Formula:C21H35NO3
  • Molecular Weight:349.514
  • Hs Code.:
  • Mol file:870640-64-5.mol
(3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate

Synonyms:(3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate

Suppliers and Price of (3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate
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
Total 3 raw suppliers
Chemical Property of (3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate
Chemical Property:
  • PSA:38.77000 
  • LogP:4.27990 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate

There total 14 articles about (3R,4S,5S)-tert-butyl 4-(benzyl(methyl)amino)-3-methoxy-5-methylheptanoate 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 boron trifluoride diethyl etherate; N,N-dimethyl-formamide; In dichloromethane; at 0 ℃; for 24.25h;
Guidance literature:
With trifluoroborane diethyl ether; In dichloromethane; N,N-dimethyl-formamide; at 0 ℃; for 24h; Inert atmosphere;
Guidance literature:
Multi-step reaction with 7 steps
1.1: sodium hydroxide / water / 0.5 h / 20 °C
2.1: sodium tetrahydroborate; water / 4 h / 5 - 20 °C
3.1: formic acid / water / 3 h / 90 °C / Inert atmosphere
4.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 - 65 °C / Inert atmosphere
5.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.75 h / -70 °C / Inert atmosphere
5.2: 1 h / -70 - -50 °C / Inert atmosphere
6.1: sulfuric acid / methanol / 0.5 h / 0 °C
6.2: 3 h / 0 - 20 °C
7.1: boron trifluoride diethyl etherate / dichloromethane; N,N-dimethyl-formamide / 24 h / 0 °C / Inert atmosphere
With sodium tetrahydroborate; lithium aluminium tetrahydride; formic acid; oxalyl dichloride; sulfuric acid; boron trifluoride diethyl etherate; water; dimethyl sulfoxide; sodium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
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