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(L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE

Base Information Edit
  • Chemical Name:(L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE
  • CAS No.:99264-69-4
  • Molecular Formula:C16H22N4O4S
  • Molecular Weight:366.441
  • Hs Code.:2933990090
  • Mol file:99264-69-4.mol
(L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE

Synonyms:Met-Pro-pNA;Metopimazine Acid;

Suppliers and Price of (L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE
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
  • American Custom Chemicals Corporation
  • (L)-METHIONYL-(L)-PROLYL-PARA-NITROANILIDE 95.00%
  • 5MG
  • $ 495.08
Total 4 raw suppliers
Chemical Property of (L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE Edit
Chemical Property:
  • PSA:146.55000 
  • LogP:2.83910 
Purity/Quality:

97% *data from raw suppliers

(L)-METHIONYL-(L)-PROLYL-PARA-NITROANILIDE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
Technology Process of (L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE

There total 5 articles about (L)-METHIONYL-(L)-PROLYL-P-NITROANILIDE 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: 90.0%

Guidance literature:
With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/j.bmcl.2013.10.071
Guidance literature:
Multi-step reaction with 2 steps
1: dicyclohexyl-carbodiimide; dmap / dichloromethane / 5 h / 20 °C
2: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
With dmap; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.bmcl.2013.10.071
Guidance literature:
Multi-step reaction with 3 steps
1: trifluoroacetic acid / dichloromethane / 1 h / 0 °C
2: dicyclohexyl-carbodiimide; dmap / dichloromethane / 5 h / 20 °C
3: trifluoroacetic acid / dichloromethane / 2 h / 20 °C
With dmap; dicyclohexyl-carbodiimide; trifluoroacetic acid; In dichloromethane;
DOI:10.1016/j.bmcl.2013.10.071
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