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15-16-monoepoxyoctadeca-9,12-dieneoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

710296-22-3

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710296-22-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 710296-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,0,2,9 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 710296-22:
(8*7)+(7*1)+(6*0)+(5*2)+(4*9)+(3*6)+(2*2)+(1*2)=133
133 % 10 = 3
So 710296-22-3 is a valid CAS Registry Number.

710296-22-3Downstream Products

710296-22-3Relevant academic research and scientific papers

UNSATURATED HYDROXY FATTY ACIDS, THE SELF DEFENSIVE SUBSTANCES IN RICE PLANT AGAINST RICE BLAST DISEASE

Kato, Tadahiro,Yamaguchi, Yoshihiro,Hirano, Takumi,Yokoyama, Toshiro,Uyehara, Tadao,et al.

, p. 409 - 412 (1984)

In addition to the previously described epoxy fatty acids, five hydroxy fatty acids were characterized as self defensive substances produced in the rice plant against rice blast disease.

Epoxidation, hydroxylation and aromatization is catalyzed by a peroxygenase from Solanum lycopersicum

Fuchs, Christopher,Schwab, Wilfried

, p. 52 - 60 (2013/10/22)

Plant peroxygenase (PXG) oxidizes unsaturated fatty acids by transferring an oxygen atom of a hydroperoxide to the double bond, thereby providing epoxides. In this work we investigated the potential of a PXG from tomato (Solanum lycopersicum, SlPXG) to catalyze the oxidation of a variety of natural products. A SlPXG gene was cloned from tomato, heterologously expressed in yeast and the membrane bound recombinant SlPXG protein was used as enzyme source. Unsaturated fatty acids, fatty acid derivatives, and terpenes were epoxidized by SlPXG in the presence of various hydroperoxides exclusively at their cis-double bonds. Terpenes with p-menthene skeleton were transformed in different ways depending on their molecular structures. R-(+)- and S-(-)-limonene were converted to R-(+)-limonene-trans-1,2-epoxide (97%) and cis-S-(-)-limonene-1,2- epoxide (88%), respectively whereas α-terpinenewas hydroxylated to cis-1,4-dihydroxy-p-menth-2-ene and γ-terpinene was aromatized to p-cymene. In the last reaction the hydroperoxide served as hydrogen acceptor rather than an oxygen donor. PXG appears to be a versatile biocatalyst able to perform different kinds of oxidation reactions. As no cofactors like NAD(P)H are required and H2O2is an environmentally friendly oxidant, PXG enables new applications for the synthesis of fine chemicals from renewable resources.

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