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15868-54-9

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15868-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15868-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,6 and 8 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15868-54:
(7*1)+(6*5)+(5*8)+(4*6)+(3*8)+(2*5)+(1*4)=139
139 % 10 = 9
So 15868-54-9 is a valid CAS Registry Number.

15868-54-9Downstream Products

15868-54-9Relevant articles and documents

Radical-Scavenging Reactions of Vitamin E and Its Model Compound, 2,2,5,7,8-Pentamethylchroman-6-ol, in a tert-Butylperoxyl Radical-Generating System

Matsuo, Mitsuyoshi,Matsumoto, Shigenobu,Iitaka, Yoichi,Niki, Etsuo

, p. 7179 - 7185 (2007/10/02)

In a tert-butylperoxyl radical-generating system containing di-tert-butyl diperoxyoxalate (DBPO) and tert-butyl hydroperoxide (BOOH), vitamin E (α-tocopherol: 1) is converted into 4a,5-epoxy-4a,5-dihydro-8a-hydroperoxy-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6(8aH)-one (2) and 8a-(tert-butyldioxy)-4a,5-epoxy-4a,5-dihydro-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6(8aH)-one (3), and its model compound 2,2,5,7,8-pentamethylchroman-6-ol (4), is converted into 4a,5-epoxy-4a,5-dihydro-8a-hydroperoxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one (5)and 8a-(tert-butyldioxy)-4a,5-epoxy-4a,5-dihydro-2,2,5,7,8-pentamethylchroman-6(8aH)-one (6).The structures of these compounds were deduced on the basis of the spectral data and, in addition, that of 5 was confirmed by X-ray crystallography.The reactions did not proceed under degassed conditions, so the presence of molecular oxygen was suggested to be a requisite for them.In the system without DBPO, 4 gives 5 and 6 in low yields, and without BOOH, 4 gives its dimers (7a and 8a) and trimer (9a).Further, it was observed that, in the presence of BOOH, 5 was derived from a hydroperoxide, 8a-hydroperoxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one (10), and was transformed into 6.Accordingly, 10 and 8a-hydroperoxy-2,5,7,8-tetramethyl-2-(4,8,12-trimethyltridecyl)chroman-6(8aH)-one (11) may be intermediates of 5 and 2, respectively, and 5 and 2 may be intermediates of 6 and 3, respectively.A possible mechanism is shown for the reaction of 1 with the tert-butylperoxyl radical (BOO.) under the hydroperoxide-rich conditions.The reaction mechanism is discussed with respect to the chain-breaking reaction of 1 against lipid peroxidation.

Reactions of a Hydroperoxide, 8a-Hydroperoxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one, Derived from a Vitamine E Model Compound: Dimerization and X-Ray Crystal Structure

Matsumoto, Shigenobu,Matsuo, Mitsuyoshi,Iitaka, Yoichi

, p. 601 - 641 (2007/10/02)

A hydroperoxide, 8a-hydroperoxy-2,2,5,7,8-pentamethylchroman-6(8aH)-one, was obtained from the reaction of a vitamin E model compound, 2,2,5,7,8-pentamethylchroman-6-ol, with singlet oxygen, and was dimerized in toluene in the presence of lead tetraacetate to give bis(2,2,5,7,8-pentamethyl-6-oxo-6,8a-dihydrochroman-8a-yl) peroxide.The structures of the hydroperoxide and peroxide were confirmed by X-ray crystallographic analysis, and their properties were examined.

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