2-iodo-N-(2-iodophenyl)benzamide

Base Information

Chemical Name:2-iodo-N-(2-iodophenyl)benzamide
CAS No.:333349-66-9
Molecular Formula:C₁₃H₉I₂NO
Molecular Weight:449.03
Hs Code.:
DSSTox Substance ID:DTXSID101301581
Nikkaji Number:J3.113.114F

Synonyms:2-iodo-N-(2-iodophenyl)benzamide;DTXSID101301581;N-(2-Iodophenyl)-2-iodobenzamide;STK062076;AKOS000459005;2-iodo-N~1~-(2-iodophenyl)benzamide;SR-01000195739;SR-01000195739-1;Z28163946;333349-66-9

Suppliers and Price of 2-iodo-N-(2-iodophenyl)benzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 2-iodo-N-(2-iodophenyl)benzamide

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:448.87736
Heavy Atom Count:17
Complexity:272

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)NC2=CC=CC=C2I)I

Technology Process of 2-iodo-N-(2-iodophenyl)benzamide

There total 2 articles about 2-iodo-N-(2-iodophenyl)benzamide 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: 53.0%

: 609-67-6
2-Iodobenzoyl chloride

: 615-43-0
2-iodophenylamine

: 333349-66-9
2-iodo-N-(2-iodophenyl)benzamide

Guidance literature:: With triethylamine; In ethyl acetate; at 20 ℃;
DOI:10.1039/b602912d

Reference yield:

: 88-67-5
2-Iodobenzoic acid

: 333349-66-9
2-iodo-N-(2-iodophenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / Reflux

2: dichloromethane / 0 - 20 °C

With thionyl chloride; In dichloromethane;
DOI:10.1055/s-0031-1289755