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2-Amino-5-iodo-N-methylbenzamide

Base Information Edit
  • Chemical Name:2-Amino-5-iodo-N-methylbenzamide
  • CAS No.:32615-70-6
  • Molecular Formula:C8H9IN2O
  • Molecular Weight:276.077
  • Hs Code.:
  • Mol file:32615-70-6.mol
2-Amino-5-iodo-N-methylbenzamide

Synonyms:

Suppliers and Price of 2-Amino-5-iodo-N-methylbenzamide
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
  • 2-AMINO-5-IODO-N-METHYLBENZAMIDE 95.00%
  • 5MG
  • $ 496.46
Total 3 raw suppliers
Chemical Property of 2-Amino-5-iodo-N-methylbenzamide Edit
Chemical Property:
  • Vapor Pressure:1.17E-05mmHg at 25°C 
  • Boiling Point:369.7°Cat760mmHg 
  • Flash Point:177.4°C 
  • PSA:58.61000 
  • Density:1.791g/cm3 
  • LogP:2.38900 
Purity/Quality:

99% *data from raw suppliers

2-AMINO-5-IODO-N-METHYLBENZAMIDE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2-Amino-5-iodo-N-methylbenzamide

There total 7 articles about 2-Amino-5-iodo-N-methylbenzamide 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:
2-amino-5-iodobenzoic acid; With 1,1'-carbonyldiimidazole; In tetrahydrofuran; for 3h; Heating / reflux;
methylamine; In tetrahydrofuran; for 2h; Heating / reflux;
Guidance literature:
With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃;
DOI:10.1039/d0ob00866d
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