1-Ethyl-3-iodobenzene

Base Information

Chemical Name:1-Ethyl-3-iodobenzene
CAS No.:19164-77-3
Molecular Formula:C8H9I
Molecular Weight:232.064
Hs Code.:
European Community (EC) Number:963-198-6
DSSTox Substance ID:DTXSID80561386
Nikkaji Number:J2.598.514A
Wikidata:Q82445176
Mol file:19164-77-3.mol

Synonyms:1-ethyl-3-iodobenzene;19164-77-3;Benzene, 1-ethyl-3-iodo-;3-Iodoethylbenzene;SCHEMBL172930;DTXSID80561386;MFCD11183303;AKOS009319828;FS-4473;CS-0358163;E78026;EN300-206175

Suppliers and Price of 1-Ethyl-3-iodobenzene

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 5 raw suppliers

Chemical Property of 1-Ethyl-3-iodobenzene

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:1
Exact Mass:231.97490
Heavy Atom Count:9
Complexity:80.6

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1=CC(=CC=C1)I

Technology Process of 1-Ethyl-3-iodobenzene

There total 3 articles about 1-Ethyl-3-iodobenzene 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%

: 17988-51-1
1-Ethyl-3-trimethylsilylbenzol

: 19164-77-3
1-ethyl-3-iodobenzene

Guidance literature:: With Iodine monochloride; In tetrachloromethane; for 48h; Heating;
DOI:10.1016/S0040-4020(01)81469-1

Reference yield: 92.0%

: 587-02-0
m-ethylaniline

: 19164-77-3
1-ethyl-3-iodobenzene

Guidance literature:: m-ethylaniline; With hydrogenchloride; In water; acetone; at 0 ℃; for 0.5h;

With sodium nitrite; In water; acetone; at 0 - 5 ℃; for 0.5h;

With potassium iodide; In water; acetone;
DOI:10.1002/ejoc.202100021

Reference yield:

: 128254-32-0
2-Ethyl-1,4-bis-trimethylsilanyl-benzene

: 19164-77-3
1-ethyl-3-iodobenzene

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / acide trifluoroacetique / CCl₄ / 15 h / Heating

2: 94 percent / monochlorure d'iode / CCl₄ / 48 h / Heating

With acide trifluoroacetique; Iodine monochloride; In tetrachloromethane;
DOI:10.1016/S0040-4020(01)81469-1