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

Base Information

Chemical Name:N-(4-Iodo-2-nitrophenyl)acetamide
CAS No.:89942-26-7
Molecular Formula:C8H7IN2O3
Molecular Weight:306.06
Hs Code.:
DSSTox Substance ID:DTXSID30476678
Nikkaji Number:J1.748.654C
Wikidata:Q82308352
Mol file:89942-26-7.mol

Synonyms:N-(4-IODO-2-NITROPHENYL)ACETAMIDE;89942-26-7;DTXSID30476678

Suppliers and Price of N-(4-Iodo-2-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

American Custom Chemicals Corporation
N-(4-IODO-2-NITROPHENYL)ACETAMIDE 95.00%
1G
$ 750.75

Total 4 raw suppliers

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

Chemical Property:

PSA：74.92000
LogP:2.75400
XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:305.95014
Heavy Atom Count:14
Complexity:241

Purity/Quality:

99% ^*data from raw suppliers

N-(4-IODO-2-NITROPHENYL)ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=C(C=C(C=C1)I)[N+](=O)[O-]

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

There total 7 articles about N-(4-Iodo-2-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: 78.0%

: 622-50-4
4-Acetamido-1-iodobenzene

: 89942-26-7
N-(4-iodo-2-nitrophenyl)acetamide

Guidance literature:: With Iron(III) nitrate nonahydrate; N-hydroxyphthalimide; In 1,2-dichloro-ethane; at 50 ℃; for 10h; regioselective reaction;
DOI:10.1039/c8ob00841h