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N-propyl-2-iodobenzamide

Base Information
  • Chemical Name:N-propyl-2-iodobenzamide
  • CAS No.:333349-52-3
  • Molecular Formula:C10H12INO
  • Molecular Weight:289.116
  • Hs Code.:
N-propyl-2-iodobenzamide

Synonyms:N-propyl-2-iodobenzamide

Suppliers and Price of N-propyl-2-iodobenzamide
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
  • 2-Iodo-N-propylbenzamide
  • 1g
  • $ 75.00
  • Crysdot
  • 2-Iodo-N-propylbenzamide 95+%
  • 10g
  • $ 395.00
  • Crysdot
  • 2-Iodo-N-propylbenzamide 95+%
  • 25g
  • $ 790.00
  • American Custom Chemicals Corporation
  • 2-IODO-N-PROPYLBENZAMIDE 95.00%
  • 5MG
  • $ 502.46
Total 3 raw suppliers
Chemical Property of N-propyl-2-iodobenzamide
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

2-Iodo-N-propylbenzamide *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of N-propyl-2-iodobenzamide

There total 3 articles about N-propyl-2-iodobenzamide 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 sodium hydroxide; In dichloromethane; at 0 - 20 ℃; for 20h;
DOI:10.3390/molecules25153354
Guidance literature:
With oxalyl dichloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20 ℃; for 1h;
DOI:10.1002/anie.201307738
Guidance literature:
Multi-step reaction with 2 steps
1: thionyl chloride / 2 h / Reflux
2: triethylamine / dichloromethane / 1 h / 20 °C
With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1016/j.tet.2019.01.023
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