4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one

Base Information

• Chemical Name: 4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one
• CAS No.: 63148-46-9
• Molecular Formula: C₁₂H₁₂N₂OS₂
• Molecular Weight: 264.372
• DSSTox Substance ID: DTXSID20494063

Synonyms:63148-46-9;DTXSID20494063;4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one

Chemical Property of 4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one

Chemical Property:

• XLogP3: 3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 3
• Exact Mass: 264.03910536
• Heavy Atom Count: 17
• Complexity: 362

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1(C(=O)SC(=N1)SC)C=NC2=CC=CC=C2

Technology Process of 4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one

There total 1 articles about 4-Methyl-2-(methylsulfanyl)-4-[(E)-(phenylimino)methyl]-1,3-thiazol-5(4H)-one 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:

4-methyl-2-methylsulfanyl-4H-thiazol-5-one (63148-45-8) + ethyl N-phenylformimidate (6780-49-0) → 4-methyl-2-methylsulfanyl-4-(phenylimino-methyl)-4H-thiazol-5-one (63148-46-9)

Guidance literature:

With pyridine; In benzene; Heating;

Reference yield:

4-methyl-2-methylsulfanyl-4-(phenylimino-methyl)-4H-thiazol-5-one (63148-46-9) → 1-methyl-3-methylsulfanyl-6-phenyl-(1rH,5cH)-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-7-one (63148-47-0,87586-86-5)

Guidance literature:

With 1H-imidazole; sodium hydride; In tetrahydrofuran; benzene;

Reference yield:

4-methyl-2-methylsulfanyl-4-(phenylimino-methyl)-4H-thiazol-5-one (63148-46-9) + tert-butylamine (75-64-9) → 5-anilino-4-methyl-2-methylsulfanyl-4,5-dihydro-thiazole-4-carboxylic acid tert-butylamide

Guidance literature:

In dichloromethane; at 25 ℃; for 0.5h;

upstream raw materials:

4-methyl-2-methylsulfanyl-4H-thiazol-5-one

ethyl N-phenylformimidate

Downstream raw materials:

1-methyl-3-methylsulfanyl-6-phenyl-(1rH,5cH)-4-thia-2,6-diaza-bicyclo[3.2.0]hept-2-en-7-one

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