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(2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester

Base Information
  • Chemical Name:(2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester
  • CAS No.:924304-81-4
  • Molecular Formula:C12H21NO4
  • Molecular Weight:243.303
  • Hs Code.:
  • Mol file:924304-81-4.mol
(2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester

Synonyms:

Suppliers and Price of (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester
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
  • TRC
  • (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylicAcidtert-ButylEster
  • 5mg
  • $ 1155.00
  • Medical Isotopes, Inc.
  • (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylicAcidtert-ButylEster
  • 100 mg
  • $ 2000.00
  • Medical Isotopes, Inc.
  • (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylicAcidtert-ButylEster
  • 10 mg
  • $ 625.00
Total 7 raw suppliers
Chemical Property of (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester
Chemical Property:
  • Solubility.:Dichloromethane, Ethyl Acetate 
Purity/Quality:

99% *data from raw suppliers

(2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylicAcidtert-ButylEster *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Uses (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester is a reactant used in the preparation of macrocyclic carboxylic acids, amides, and acylsulfonamides as inhibitors of HCV replication.
Technology Process of (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester

There total 16 articles about (2S,4R)-4-Ethyl-1,2-pyrrolidinedicarboxylic Acid tert-Butyl Ester 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 palladium 10% on activated carbon; hydrogen; In methanol; at 20 ℃;
Guidance literature:
With hydrogen; palladium 10% on activated carbon; In ethanol; Inert atmosphere;
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