Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate

Base Information

Chemical Name:Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate
CAS No.:91393-36-1
Molecular Formula:C12H12N2O3S
Molecular Weight:264.305
Hs Code.:
DSSTox Substance ID:DTXSID50576245
Nikkaji Number:J510.088G

Synonyms:DTXSID50576245;Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate

Suppliers and Price of Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate

Supply Marketing:

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

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Chemical Property of Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:264.05686342
Heavy Atom Count:18
Complexity:366

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(=O)C1C(=O)N(C(=S)N1)C2=CC=CC=C2

Technology Process of Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate

There total 4 articles about Ethyl 5-oxo-1-phenyl-2-sulfanylideneimidazolidine-4-carboxylate 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: 90.0%

: 96749-36-9
N-dicarbethoxy-methyl N'-phenyl thiouree

: 91393-36-1
5-carbethoxy 3-phenyl-2-thio hydantoine

Guidance literature:: With sulfuric acid; In ethanol; for 12h; Ambient temperature;
DOI:10.1016/0223-5234(92)90011-O

Reference yield:

: 6829-40-9
aminomalonic acid diethyl ester

: 91393-36-1
5-carbethoxy 3-phenyl-2-thio hydantoine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / ethanol / 24 h / Ambient temperature

2: 90 percent / 4percent H₂SO₄ / ethanol / 12 h / Ambient temperature

With sulfuric acid; In ethanol;
DOI:10.1016/0223-5234(92)90011-O

Reference yield:

: 103-72-0
phenyl isothiocyanate

: 91393-36-1
5-carbethoxy 3-phenyl-2-thio hydantoine

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / ethanol / 24 h / Ambient temperature

2: 90 percent / 4percent H₂SO₄ / ethanol / 12 h / Ambient temperature

With sulfuric acid; In ethanol;
DOI:10.1016/0223-5234(92)90011-O