4-(Furan-2-yl)-2-phenyl-1,3-thiazole

Base Information

Chemical Name:4-(Furan-2-yl)-2-phenyl-1,3-thiazole
CAS No.:21036-63-5
Molecular Formula:C13H9NOS
Molecular Weight:227.287
Hs Code.:
DSSTox Substance ID:DTXSID40571380
Nikkaji Number:J2.112.085E
Wikidata:Q82459454

Synonyms:21036-63-5;4-(Furan-2-yl)-2-phenyl-1,3-thiazole;DTXSID40571380

Suppliers and Price of 4-(Furan-2-yl)-2-phenyl-1,3-thiazole

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4-(Furan-2-yl)-2-phenyl-1,3-thiazole

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:227.04048508
Heavy Atom Count:16
Complexity:230

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC(=CS2)C3=CC=CO3

Technology Process of 4-(Furan-2-yl)-2-phenyl-1,3-thiazole

There total 6 articles about 4-(Furan-2-yl)-2-phenyl-1,3-thiazole 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: 74.0%

: 15109-94-1
1-(2-furyl)-2-bromoethanone

: 2227-79-4
benzenecarbothioamide

: 21036-63-5
4-(2-furyl)-2-phenylthiazole

Guidance literature:: In tetrahydrofuran; Reflux;
DOI:10.1021/jo102081a

Reference yield: 73.0%

: 17678-19-2
2-(2-hydroxyacetyl)furan

: 2227-79-4
benzenecarbothioamide

: 21036-63-5
4-(2-furyl)-2-phenylthiazole

Guidance literature:: 2-(2-hydroxyacetyl)furan; With triethylamine; In dichloromethane; for 24h; Heating;

benzenecarbothioamide; With potassium carbonate; In acetonitrile; for 10h; Further stages.; Heating;
DOI:10.1080/00397910802136672