Thiophene, 5-chloro-2-iodo-3-phenyl-

Base Information

Chemical Name:Thiophene, 5-chloro-2-iodo-3-phenyl-
CAS No.:143203-11-6
Molecular Formula:C10H6ClIS
Molecular Weight:320.581
Hs Code.:
DSSTox Substance ID:DTXSID30455968
Wikidata:Q82278147
Mol file:143203-11-6.mol

Synonyms:Thiophene, 5-chloro-2-iodo-3-phenyl-;143203-11-6;DTXSID30455968

Suppliers and Price of Thiophene, 5-chloro-2-iodo-3-phenyl-

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 1 raw suppliers

Chemical Property of Thiophene, 5-chloro-2-iodo-3-phenyl-

Chemical Property:

XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:319.89235
Heavy Atom Count:13
Complexity:170

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=C(SC(=C2)Cl)I

Technology Process of Thiophene, 5-chloro-2-iodo-3-phenyl-

There total 2 articles about Thiophene, 5-chloro-2-iodo-3-phenyl- 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: 17.0%

: 35717-21-6
2-chloro-4-phenylthiophene

: 143203-11-6
5-chloro-2-iodo-3-phenylthiophene

: 5-chloro-2-nitro-3-phenylthiophene

Guidance literature:: With acetic acid; potassium nitrate; potassium iodide; for 0.5h; Heating;
DOI:10.1246/bcsj.67.2187

Reference yield:

: 2404-87-7
3-phenylthiophene

: 143203-11-6
5-chloro-2-iodo-3-phenylthiophene

Guidance literature:: Multi-step reaction with 2 steps

1: SO₂Cl₂ / CCl₄ / 8 h / Heating

2: 78 percent / KI, KNO₃, acetic acid / 0.5 h / Heating

With sulfuryl dichloride; acetic acid; potassium nitrate; potassium iodide; In tetrachloromethane;
DOI:10.1246/bcsj.67.2187