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Tetrahydro-3-(2-phenylethyl)-2-thioxo-4H-1,3-thiazin-4-on is a complex organic compound with the molecular formula C13H15NOS2. It is a derivative of the 1,3-thiazine class of heterocyclic compounds, characterized by the presence of a sulfur atom and a nitrogen atom in the ring structure. This specific compound features a tetrahydro (four hydrogen atoms attached to a carbon atom) and a 2-thioxo (a sulfur atom double-bonded to an oxygen atom) functional groups. The 2-phenylethyl side chain, which is a benzene ring attached to an ethyl group, further adds to its structural complexity. Tetrahydro-3-(2-phenylethyl)-2-thioxo-4H-1,3-thiazin-4-on may have potential applications in pharmaceuticals or as a chemical intermediate, but its specific uses and properties would depend on further research and characterization.

4094-49-9

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4094-49-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4094-49-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,9 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4094-49:
(6*4)+(5*0)+(4*9)+(3*4)+(2*4)+(1*9)=89
89 % 10 = 9
So 4094-49-9 is a valid CAS Registry Number.

4094-49-9Relevant academic research and scientific papers

Solvent free one-pot synthesis of 2-thioxo-1,3-thiazinane-4-one derivatives

Nasiri, Farough,Zolali, Amin,Ahmadiazar, Mohammad

, p. 180 - 184 (2014/01/06)

An efficient one-pot synthesis of 2-thioxo-1,3-thiazinane-4-one derivatives through the reaction of primary amines and carbon disulfide in the presence of acryloyl chloride is described. This reaction is carried out under solvent-free condition and withou

Investigations on 1,3-Thiazines, 17. - About the Reaction of N-monosubstituted Dithiocarbamates with α,β-Unsaturated Carboxylic Acid Chlorides

Hanefeld, Wolfgang,Glaeske, Gerd

, p. 1388 - 1393 (2007/10/02)

The reaction of N-monosubstituted dithiocarbamates with α,β-unsaturated carboxylic acid chlorides yields, depending on the nature of the nitrogen substituent of the dithiocarbamate, the substituents of the acid chloride, and the reaction conditions, eithe

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