4-Iodoanilinium chloride

Base Information

Chemical Name:4-Iodoanilinium chloride
CAS No.:74367-81-0
Molecular Formula:C6H6 I N . Cl H
Molecular Weight:255.486
Hs Code.:2921420090
European Community (EC) Number:277-842-2
DSSTox Substance ID:DTXSID30225365
Mol file:74367-81-0.mol

Synonyms:4-Iodoanilinium chloride;4-iodoaniline hydrochloride;74367-81-0;4-iodoaniline;hydrochloride;EINECS 277-842-2;p-Iodoaniline, hydrochloride;C6H6IN.ClH;C6-H6-I-N.Cl-H;SCHEMBL7893866;DTXSID30225365;FT-0618777;FT-0618778;ETHYL6-METHYL-2-OXO-4-PHENYL-1,2-DIHYDRO-5-PYRIMIDINECARBOXYLATE

Suppliers and Price of 4-Iodoanilinium chloride

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
4-IODOANILINE HYDROCHLORIDE 95.00%
5MG
$ 504.24

Total 6 raw suppliers

Chemical Property of 4-Iodoanilinium chloride

Chemical Property:

Vapor Pressure:0.00758mmHg at 25°C
Boiling Point:268.7°C at 760 mmHg
Flash Point:116.3°C
PSA：26.02000
LogP:3.25660
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:254.93117
Heavy Atom Count:9
Complexity:66.9

Purity/Quality:

98%Min ^*data from raw suppliers

4-IODOANILINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N)I.Cl

Technology Process of 4-Iodoanilinium chloride

There total 7 articles about 4-Iodoanilinium chloride 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: 94.0%

: C₂₂H₁₄INO₂

: 4808-48-4
2,3-diphenylmaleic anhydride

: 74367-81-0
4-iodoaniline hydrochloride

Guidance literature:: C₂₂H₁₄INO₂; With potassium hydroxide; In ethanol; water; at 80 ℃; for 2h; Green chemistry;

With hydrogenchloride; In ethanol; water; pH=4; Green chemistry;
DOI:10.1039/c6gc01318j

Reference yield: 86.0%

: 636-98-6
p-nitrobenzene iodide

: 74367-81-0
4-iodoaniline hydrochloride

Guidance literature:: p-nitrobenzene iodide; With iododioxobis(triphenylphosphine)rhenium(V); Dimethylphenylsilane; In toluene; for 1.5h; Reflux;

With hydrogenchloride; In diethyl ether; toluene;
DOI:10.1021/jo9008657

Reference yield:

: 1-(4-aminophenyl)-3,4-diphenyl-1H-pyrrole-2,5-dione

: 4808-48-4
2,3-diphenylmaleic anhydride

: 74367-81-0
4-iodoaniline hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride; sodium nitrite / water; N,N-dimethyl-formamide / 0.33 h / 0 °C

2.1: potassium iodide / water; N,N-dimethyl-formamide / 0.5 h / 50 °C

3.1: potassium hydroxide / ethanol; water / 2 h / 80 °C / Green chemistry

3.2: pH 4 / Green chemistry

With hydrogenchloride; potassium iodide; potassium hydroxide; sodium nitrite; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1039/c6gc01318j