DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

Base Information

Chemical Name:DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid
CAS No.:102768-06-9
Molecular Formula:C₂₂H₃₄N₂O₄
Molecular Weight:390.523
Hs Code.:

Synonyms:DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

Suppliers and Price of DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

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 0 raw suppliers

Chemical Property of DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

There total 2 articles about DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid 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:

Reference yield: 46.0%

: 111-92-2
dibutylamine

: 102743-18-0
3,4-dimethyl-N-benzoyl-DL-glutamic anhydride

: 97964-53-9
(+/-)-CR 1372

: 102768-06-9
DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

Guidance literature:: In water; at 5 - 10 ℃; for 3h;

Reference yield:

: 102743-17-9
3,4-dimethyl-N-benzoyl-DL-glutamic acid

: 102768-06-9
DL-2-(3,4-dimethyl-benzoyl-amino)-5-(di-n-butyl-amino)-5-oxo-pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 82.5 percent / acetic anhydride / diisopropyl ether / 2 h / 70 °C

2: 28.8 percent / tetrahydrofuran / 3 h / 25 °C

With acetic anhydride; In tetrahydrofuran; di-isopropyl ether;