5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione

Base Information

• Chemical Name: 5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione
• CAS No.: 79835-72-6
• Molecular Formula: C₁₂H₁₆N₂O₂S
• Molecular Weight: 252.337
• NSC Number: 120811
• DSSTox Substance ID: DTXSID20388776

Synonyms:79835-72-6;NSC120811;DTXSID20388776;Athyl-cyclohexenyl-thiobarbitursaure;NSC-120811;5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione

Chemical Property of 5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Density: 1.27g/cm³
• XLogP3: 2.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 252.09324893
• Heavy Atom Count: 17
• Complexity: 395

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC1(C(=O)NC(=S)NC1=O)C2=CCCCC2

Technology Process of 5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione

There total 1 articles about 5-(Cyclohex-1-en-1-yl)-5-ethyl-2-sulfanylidenedihydropyrimidine-4,6(1H,5H)-dione 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:

5-ethyl-6-amino-5-cyclohex-1-enyl-2-thioxo-2,5-dihydro-3H-pyrimidin-4-one (6297-73-0) → 5-Ethyl-5--2-thio-barbitursaeure (79835-72-6)

Guidance literature:

With sulfuric acid;

Reference yield:

5-Ethyl-5--2-thio-barbitursaeure (79835-72-6) → (5-ethyl-5-cyclohex-1-enyl-4,6-dioxo-1,4,5,6-tetrahydro-pyrimidin-2-ylmercapto)-acetic acid

Guidance literature:

With sodium monochloroacetic acid;

upstream raw materials:

5-ethyl-6-amino-5-cyclohex-1-enyl-2-thioxo-2,5-dihydro-3H-pyrimidin-4-one

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