2-iodo-N-(4-nitrophenyl)acetamide

Base Information

Chemical Name:2-iodo-N-(4-nitrophenyl)acetamide
CAS No.:76809-64-8
Molecular Formula:C8H7IN2O3
Molecular Weight:306.06
Hs Code.:
DSSTox Substance ID:DTXSID501299275

Synonyms:2-iodo-N-(4-nitrophenyl)acetamide;DTXSID501299275;N-(4-nitrophenyl)-2-iodoacetamide;AKOS014117606;76809-64-8

Suppliers and Price of 2-iodo-N-(4-nitrophenyl)acetamide

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

Total 0 raw suppliers

Chemical Property of 2-iodo-N-(4-nitrophenyl)acetamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:305.95014
Heavy Atom Count:14
Complexity:221

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1NC(=O)CI)[N+](=O)[O-]

Technology Process of 2-iodo-N-(4-nitrophenyl)acetamide

There total 1 articles about 2-iodo-N-(4-nitrophenyl)acetamide 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: 68.0%

: 17329-87-2
2-chloro-N-(4-nitro-phenyl)-acetamide

: 76809-64-8
4-nitrophenyl iodoacetamide

Guidance literature:: With sodium iodide;
DOI:10.1248/cpb.28.2720

Reference yield: 37.0%

: 622-32-2
(Z)-benzaldehyde oxime

: 76809-64-8
4-nitrophenyl iodoacetamide

: 76809-85-3
C₁₅H₁₃N₃O₄

Guidance literature:: With sodium ethanolate; In ethanol; Ambient temperature;
DOI:10.1248/cpb.28.2720

Reference yield:

: 76809-64-8
4-nitrophenyl iodoacetamide

: 76810-04-3
2-Hydroxyamino-N-(4-nitro-phenyl)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 37 percent / NaOEt / ethanol / Ambient temperature

2: 44 percent / conc HCl / methanol / 2 h / 50 °C

With hydrogenchloride; sodium ethanolate; In methanol; ethanol;
DOI:10.1248/cpb.28.2720