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4-(p-tolyl)-3H-1,2-dithiol-3-one is an organic compound characterized by its unique structure, which features a 1,2-dithiol-3-one core with a p-tolyl group attached at the 4-position. This molecule is composed of a heterocyclic ring system containing sulfur atoms, which contribute to its reactivity and potential applications in various chemical processes. The p-tolyl group, a substituted phenyl ring with a methyl group at the para position, influences the compound's electronic properties and steric effects. This chemical is of interest in the field of organic synthesis, potentially serving as a building block for more complex molecules or as a reagent in chemical transformations. Its properties, such as solubility, stability, and reactivity, make it a candidate for further study in the development of new materials or pharmaceuticals.

3467-28-5

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3467-28-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3467-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,6 and 7 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3467-28:
(6*3)+(5*4)+(4*6)+(3*7)+(2*2)+(1*8)=95
95 % 10 = 5
So 3467-28-5 is a valid CAS Registry Number.

3467-28-5Upstream product

3467-28-5Relevant academic research and scientific papers

Selective [3 + 2] Cycloaddition of Cyclopropenone Derivatives and Elemental Chalcogens

Wu, Jian,Gao, Wen-Xia,Huang, Xiao-Bo,Zhou, Yun-Bing,Liu, Miao-Chang,Wu, Hua-Yue

supporting information, p. 5555 - 5560 (2020/07/30)

A highly efficient method is disclosed for the synthesis of 1,2-dichalcogen heterocycles via [3 + 2] cycloaddition of cyclopropenone derivatives and elemental chalcogens. Different from other cyclopropenone derivatives, cyclopropenselenones undergo unprec

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