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2-(2,5-Dimethyl-phenoxy)-[1,3,5]trithiane is an organic compound with the molecular formula C11H14OS3. It is a colorless to pale yellow liquid with a molecular weight of 246.43 g/mol. 2-(2,5-Dimethyl-phenoxy)-[1,3,5]trithiane is characterized by its unique structure, which consists of a phenoxy group attached to a trithiane backbone. The phenoxy group has two methyl groups at the 2 and 5 positions, which contribute to its chemical properties. It is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals, as well as in the production of dyes and pigments. Due to its potential applications and reactivity, it is important to handle 2-(2,5-Dimethyl-phenoxy)-[1,3,5]trithiane with care, following proper safety protocols.

81259-20-3

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81259-20-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81259-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,5 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 81259-20:
(7*8)+(6*1)+(5*2)+(4*5)+(3*9)+(2*2)+(1*0)=123
123 % 10 = 3
So 81259-20-3 is a valid CAS Registry Number.

81259-20-3Downstream Products

81259-20-3Relevant academic research and scientific papers

Synthesis and Reactions of 2-Aryloxy-s-trithianes

Walther, H.,Gross, H.

, p. 939 - 950 (2007/10/02)

2-Aryloxy-s-trithianes 4 had been prepared from 1-tosyl-imino-1-SIV-1,3,5-trithiane and phenolates. - By self-condensation of 4 1,5-bis-(trithianyl)-1,3,5-trithiapentane 5 and triphenylorthoformate 7 are formed, accompanied by further products, which had been isolated in pure state and identified unambiguously by H-n.m.r. and mass-spectra.In the presence of acids the 2-aryloxy-s-trithianes 4 react with nucleophilic aromatic compounds such as phenoles, N,N-dimethylaniline, pyrrole, indole, and thiophenes to give the C-trithianylated products.With mercaptanes 2-alkylthio-s-trithianes are formed.

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