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N-(2-iodophenyl)-N-methylacetamide

Base Information Edit
  • Chemical Name:N-(2-iodophenyl)-N-methylacetamide
  • CAS No.:90585-26-5
  • Molecular Formula:C9H10INO
  • Molecular Weight:275.089
  • Hs Code.:
  • DSSTox Substance ID:DTXSID40524452
  • Nikkaji Number:J848.835E
  • Wikidata:Q82391328
  • Mol file:90585-26-5.mol
N-(2-iodophenyl)-N-methylacetamide

Synonyms:N-(2-iodophenyl)-N-methylacetamide;90585-26-5;SCHEMBL19155104;DTXSID40524452

Suppliers and Price of N-(2-iodophenyl)-N-methylacetamide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-(2-iodophenyl)-N-methylacetamide Edit
Chemical Property:
  • XLogP3:1.9
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:1
  • Exact Mass:274.98071
  • Heavy Atom Count:12
  • Complexity:172
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)N(C)C1=CC=CC=C1I
Technology Process of N-(2-iodophenyl)-N-methylacetamide

There total 4 articles about N-(2-iodophenyl)-N-methylacetamide 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:
o-iodobenzanilide; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.583333h; Inert atmosphere;
methyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.8b02819
Guidance literature:
With tributylphosphine; sodium iodide; nickel dibromide; In 1-methyl-pyrrolidin-2-one; at 190 ℃; for 7h; Inert atmosphere; Molecular sieve; Sealed tube;
DOI:10.1039/c2cc30956d
Guidance literature:
Multi-step reaction with 2 steps
1: 1.02 g / pyridine / CH2Cl2 / 12 h / 20 °C
2: 680 mg / NaH / tetrahydrofuran; various solvent(s) / 21 h / 20 °C
With pyridine; sodium hydride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ol061858h
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