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3-Benzyltetrahydro-2-thioxo-4H-1,3-thiazin-4-on is a chemical compound with the molecular formula C11H13NOS2. It is a heterocyclic compound belonging to the class of 1,3-thiazines, which are characterized by a six-membered ring containing two sulfur atoms and one nitrogen atom. The compound features a benzyl group attached to the 3-position of the thiazine ring, and a thioxo group (a sulfur-oxygen double bond) at the 2-position. This molecule is of interest in organic chemistry and may have potential applications in the synthesis of pharmaceuticals and other chemical products. Its structure and properties make it a versatile building block for the development of new compounds with various biological activities.

4094-48-8

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4094-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4094-48-8 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 4094-48:
(6*4)+(5*0)+(4*9)+(3*4)+(2*4)+(1*8)=88
88 % 10 = 8
So 4094-48-8 is a valid CAS Registry Number.

4094-48-8Relevant 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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