5-Ethyl-2-phenyl-4,5-dihydro-1,3-thiazole

Base Information

Chemical Name:5-Ethyl-2-phenyl-4,5-dihydro-1,3-thiazole
CAS No.:6638-36-4
Molecular Formula:C11H13 N S
Molecular Weight:191.29
Hs Code.:2934100090
NSC Number:48050
DSSTox Substance ID:DTXSID90286856
Nikkaji Number:J402.246G
Mol file:6638-36-4.mol

Synonyms:6638-36-4;5-ethyl-2-phenyl-4,5-dihydro-1,3-thiazole;NSC48050;DTXSID90286856;NSC-48050

Suppliers and Price of 5-Ethyl-2-phenyl-4,5-dihydro-1,3-thiazole

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 5-Ethyl-2-phenyl-4,5-dihydro-1,3-thiazole

Chemical Property:

Vapor Pressure:0.00192mmHg at 25°C
Boiling Point:301.1°C at 760 mmHg
Flash Point:135.9°C
PSA：37.66000
Density:1.11g/cm³
LogP:2.39420
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:191.07687059
Heavy Atom Count:13
Complexity:194

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1CN=C(S1)C2=CC=CC=C2

Technology Process of 5-Ethyl-2-phenyl-4,5-dihydro-1,3-thiazole

There total 6 articles about 5-Ethyl-2-phenyl-4,5-dihydro-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: 83.0%

: 133523-84-9
2-Phenyl-5-(1-phenylselanyl-ethyl)-4,5-dihydro-thiazole

: 6638-36-4
5-Ethyl-2-phenyl-2-thiazoline

Guidance literature:: With triphenylstannane; 2,2'-azobis(isobutyronitrile); for 2h;
DOI:10.1021/jo00010a045

Reference yield: 80.0%

: 133523-74-7
N-crotyl-thiobenzamide

: 6638-36-4
5-Ethyl-2-phenyl-2-thiazoline

Guidance literature:: toluene-4-sulfonic acid; In toluene; for 20h; Heating;
DOI:10.1021/jo00010a045

Reference yield:

: 133523-72-5,157830-13-2
N-benzoyl-(E)-1-amino-2-butene

: 6638-36-4
5-Ethyl-2-phenyl-2-thiazoline

Guidance literature:: Multi-step reaction with 3 steps

1: 82 percent / Lawesson's reagent / tetrahydrofuran / Heating

2: CHCl₃ / 3 h

3: 83 percent / Ph₃SnH / AIBN / 2 h

With Lawessons reagent; triphenylstannane; 2,2'-azobis(isobutyronitrile); In tetrahydrofuran; chloroform;
DOI:10.1021/jo00010a045