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2-(1',2-epoxyethyl-1'-phenylsulfoxy)-4a-methyl-1,2,3,4,4a,5,6,7-octahydronaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

313478-13-6

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313478-13-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 313478-13-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,4,7 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 313478-13:
(8*3)+(7*1)+(6*3)+(5*4)+(4*7)+(3*8)+(2*1)+(1*3)=126
126 % 10 = 6
So 313478-13-6 is a valid CAS Registry Number.

313478-13-6Downstream Products

313478-13-6Relevant academic research and scientific papers

Synthesis and allergenic potential of a 15-hydroperoxyabietic acid-like model: Trapping of radical intermediates

Mutterer,Gimenez Arnau,Karlberg,Lepoittevin

, p. 1028 - 1036 (2000)

To better understand the skin sensitization mechanism of 15-hydroperoxyabietic acid-like compounds, 2-(1'-hydroperoxy-1'-methylethyl)-4a-methyl-3,4,4a,5,6,7-hexahydronaphthalene 7 was synthesized. The allergenic activity of this compound was tested on mice using the local lymph node assay, and further evaluated on guinea pigs using the Freund's complete adjuvant test. Using these methods, hydroperoxide 7 was found to be a strong sensitizer. Radical-trapping experiments were carried out on this compound in the presence of the spin-trapping agent, 1,1,3,3-tetramethylisoindolin-2-yloxyl 17, using light to induce radicals. The formation of carbon-centered radicals derived from compound 7 by intramolecular cyclization of an oxygen-centered radical was observed. The reaction of these intermediates with 17 gave various adducts in a very low yield, but a 1/1 mixture of diastereomers 18a and 18b (0.1% yield) was isolated and characterized, together with compound 19 (0.03% yield). The results suggest that carbon-centered reactive radicals are formed from allylic hydroperoxides and that this could be the possible mechanism involved in allergic contact dermatitis to abietic acid.

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