2-chloro-N-(3-iodophenyl)acetamide

Base Information

Chemical Name:2-chloro-N-(3-iodophenyl)acetamide
CAS No.:2564-01-4
Molecular Formula:C8H7 Cl I N O
Molecular Weight:295.5
Hs Code.:
European Community (EC) Number:846-785-0
DSSTox Substance ID:DTXSID30368185
Wikidata:Q82154551
Mol file:2564-01-4.mol

Synonyms:2-chloro-N-(3-iodophenyl)acetamide;2564-01-4;2-Chloro-N-(3-iodo-phenyl)-acetamide;Acetamide,2-chloro-N-(3-iodophenyl)-;DTXSID30368185;CAA56401;STK804776;AKOS000400699;EN300-01795;Z56824475

Suppliers and Price of 2-chloro-N-(3-iodophenyl)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
2-CHLORO-N-(3-IODO-PHENYL)-ACETAMIDE 95.00%
500MG
$ 784.25

AK Scientific
2-Chloro-N-(3-iodophenyl)acetamide
1g
$ 679.00

Total 4 raw suppliers

Chemical Property of 2-chloro-N-(3-iodophenyl)acetamide

Chemical Property:

PSA：29.10000
LogP:2.54150
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:294.92609
Heavy Atom Count:12
Complexity:165

Purity/Quality:

99% ^*data from raw suppliers

2-CHLORO-N-(3-IODO-PHENYL)-ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)I)NC(=O)CCl

Technology Process of 2-chloro-N-(3-iodophenyl)acetamide

There total 2 articles about 2-chloro-N-(3-iodophenyl)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: 82.0%

: 79-04-9
chloroacetyl chloride

: 626-01-7
3-Iodoaniline

: 2564-01-4
PCM-0102154

Guidance literature:: With sodium hydrogencarbonate; In 1,4-dioxane; for 0.5h;
DOI:10.1007/BF00758665

Reference yield:

: 2564-01-4
PCM-0102154

Guidance literature:: Aus Chloressigsaeure, 1) Keten, 2) 3-Iod-anilin;

Reference yield:

: 2564-01-4
PCM-0102154

: 81112-68-7
N-(3-Iodo-phenyl)-2-piperidin-1-yl-acetamide; compound with oxalic acid

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 2 h / Heating

2: diethyl ether

In diethyl ether; acetone;
DOI:10.1007/BF00758665