4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-

Base Information

Chemical Name:4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-
CAS No.:79421-55-9
Molecular Formula:C₁₁H₉NO₂S
Molecular Weight:219.264
Hs Code.:
DSSTox Substance ID:DTXSID70393976
Wikidata:Q82193089

Synonyms:4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-;79421-55-9;DTXSID70393976;AKOS005362293

Suppliers and Price of 4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-

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 4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:219.03539970
Heavy Atom Count:15
Complexity:306

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1C(=O)N=C(S1)CC(=O)C2=CC=CC=C2

Technology Process of 4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)-

There total 2 articles about 4(5H)-Thiazolone, 2-(2-oxo-2-phenylethyl)- 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: 75.0%

: 68-11-1
mercaptoacetic acid

: 91132-63-7
(E)-3-Amino-3-ethoxy-1-phenyl-2-propen-1-on

: 79421-55-9
4-Oxo-2-phenacyl-4,5-dihydrothiazole

Guidance literature:: In acetic acid; for 3h; Heating;
DOI:10.1055/s-1989-27393

Reference yield:

: 614-16-4
Benzoylacetonitrile

: 79421-55-9
4-Oxo-2-phenacyl-4,5-dihydrothiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / 1.) HCl, 2.) Et₃N / 1.) Et₂₀, 0 degC, 6 h, 2.) water, 15 min

2: 75 percent / acetic acid / 3 h / Heating

With hydrogenchloride; triethylamine; In acetic acid;
DOI:10.1055/s-1989-27393