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(Z)-2-phenylsulfonylmethylenethiazolidin-4-one is a chemical compound with the molecular formula C10H8NO3S2. It is a derivative of thiazolidin-4-one, featuring a phenylsulfonyl group attached to the methylene carbon in the (Z)-configuration. (Z)-2-phenylsulfonylmethylenethiazolidin-4-one is known for its potential applications in organic synthesis and as a building block for the development of pharmaceuticals and other chemical products. Its structure provides a unique reactivity profile, which can be exploited in various chemical transformations. The compound's properties, such as its stability and reactivity, make it a valuable intermediate in the synthesis of more complex molecules.

24146-39-2

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24146-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24146-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,1,4 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24146-39:
(7*2)+(6*4)+(5*1)+(4*4)+(3*6)+(2*3)+(1*9)=92
92 % 10 = 2
So 24146-39-2 is a valid CAS Registry Number.

24146-39-2Downstream Products

24146-39-2Relevant academic research and scientific papers

A facile strategy for the annulation of 2-phenylsulfonyl methylene thiazolidin-4-one via multicomponent reactions

Altu?, Cevher,Caner, Esra

, p. 217 - 221 (2013/05/09)

An efficient synthesis of 5-amino-7-aryl-3-oxo-8-(phenylsulfonyl)- thiazolo[3,2-a]pyridine-6-carbonitriles was conducted utilizing multicomponent condensation reaction of malononitrile, aromatic aldehydes and 2-phenylsulfonylmethylenethiazolidin-4-one in one pot. Depending on the equivalence of the aldehyde, two different products were obtained from moderate to excellent yields. Thirteen novel structures were characterized by physical and spectroscopic methods (m.p., Rf, IR, NMR and mass analysis).

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