2-Ethyl-2-methyl-4-phenyl-3-thiazoline

Base Information

Chemical Name:2-Ethyl-2-methyl-4-phenyl-3-thiazoline
CAS No.:91642-80-7
Molecular Formula:C₁₂H₁₅NS
Molecular Weight:205.324
Hs Code.:
DSSTox Substance ID:DTXSID70919615

Synonyms:2-Ethyl-2-methyl-4-phenyl-3-thiazoline;BRN 0006526;3-Thiazoline, 2-ethyl-2-methyl-4-phenyl-;Thiazole, 2-ethyl-2,5-dihydro-2-methyl-4-phenyl-;91642-80-7;4-27-00-01122 (Beilstein Handbook Reference);DTXSID70919615;2-Ethyl-2-methyl-4-phenyl-2,5-dihydro-1,3-thiazole

Suppliers and Price of 2-Ethyl-2-methyl-4-phenyl-3-thiazoline

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 2-Ethyl-2-methyl-4-phenyl-3-thiazoline

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:205.09252066
Heavy Atom Count:14
Complexity:231

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1(N=C(CS1)C2=CC=CC=C2)C

Technology Process of 2-Ethyl-2-methyl-4-phenyl-3-thiazoline

There total 3 articles about 2-Ethyl-2-methyl-4-phenyl-3-thiazoline 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: 64.0%

: 2461-75-8
benzoylmethyl disulfide

: 78-93-3
butanone

: 91642-80-7
ethyl-2 methyl-2 phenyl-4 Δ-3 thiazoline

Guidance literature:: With hydrogen sulfide; ammonia; In diethyl ether; for 5h;

Reference yield:

: 70-11-1
α-bromoacetophenone

: 91642-80-7
ethyl-2 methyl-2 phenyl-4 Δ-3 thiazoline

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) sodium thiosulphate; 2.) H₂SO₄, H₂O₂ / 1.) methanol, water, reflux, 2 h; 2.) acetone, 24 h

2: 64 percent / H₂S, NH₃ / diethyl ether / 5 h

With sulfuric acid; hydrogen sulfide; ammonia; dihydrogen peroxide; sodium thiosulfate; In diethyl ether;