221633-52-9

Usage

Uses

Further research and analysis would be necessary to fully understand the properties and potential uses of (11S,12S,13S)-(9Z,15Z)-11-Hydroxy-12,13-epoxyoctadeca-9,15-dienoic acid methyl ester. However, based on its structure and functional groups, it may have potential applications in various industries, such as:
Used in Pharmaceutical Industry:
(11S,12S,13S)-(9Z,15Z)-11-Hydroxy-12,13-epoxyoctadeca-9,15-dienoic acid methyl ester may be used as a pharmaceutical agent for its potential biological activities or functions. The hydroxy and epoxy groups may allow for interactions with other molecules, making it a promising candidate for drug development.
Used in Chemical Industry:
(11S,12S,13S)-(9Z,15Z)-11-Hydroxy-12,13-epoxyoctadeca-9,15-dienoic acid methyl ester may be used as a chemical intermediate or reactant in the synthesis of other compounds due to its reactivity and potential interactions with other molecules.
Used in Cosmetic Industry:
(11S,12S,13S)-(9Z,15Z)-11-Hydroxy-12,13-epoxyoctadeca-9,15-dienoic acid methyl ester may be used as an ingredient in cosmetic products for its potential moisturizing, emollient, or other beneficial properties.

Upstream product

• 150311-79-8 ethyl 11(S),12(R)-O-isopropylidene-11,12,13(R)-trihydroxy-octadeca-9,15(Z)-dienoate 
• 205380-49-0 (12E,15Z)-11-(Triethylsilyloxy)octadeca-12,15-dien-9-ynoic acid methyl ester 
• 205380-50-3 (9Z,12E,15Z)-11-(Triethylsilyloxy)octadeca-9,12,15-trienoic acid methyl ester 
• 205380-43-4 (3Z,6E)-8-Acetoxy-18-(tert-butyldimethylsilyloxy)octadeca-3,6-dien-9-yne 
• 205380-47-8 (12E,15Z)-11-Acetoxyoctadeca-12,15-dien-9-ynoic acid methyl ester 
• 205380-46-7 (12E,15Z)-11-Acetoxyoctadeca-12,15-dien-9-ynoic acid 
• 205380-42-3 (3Z,6E)-18-(tert-Butyldimethylsilyloxy)octadeca-3,6-dien-9-yn-8-ol 
• 205380-48-9 (12E,15Z)-11-Hydroxyoctadeca-12,15-dien-9-ynoic acid methyl ester 
• 205380-45-6 (12E,15Z)-11-Acetoxyoctadeca-12,15-dien-9-yn-1-al 
• 205380-44-5 (12E,15Z)-11-Acetoxyoctadeca-12,15-dien-9-yn-1-ol 
• 205380-41-2 (2E,5Z)-Octa-2,5-dienal 
• 75958-90-6 (2E,5Z)-Octa-2,5-dienoic acid ethyl ester 
• 67548-36-1 (2E,5Z)-Octa-2,5-dien-1-ol 
• 6789-80-6 (3Z)-hexenal 

Relevant academic research and scientific papers

Enantiocontrolled synthesis of naturally occuring octadecadienoic acid derivatives, self-defensive substances against rice blast disease, by means of the Sharpless asymmetric epoxidation of unsymmetrical divinylmethanol

(11S,121S,13S)-(9Z,15Z)- and (11R,12S,13S)-(9Z,15Z)-11-hydroxy-12,13-epoxyoctadecadienoic acids and (11R,12S,13S)-(9Z,15Z)-11,12,13-trihydroxyoctadecadienoic acid, self-defensive substances against the rice blast disease, were synthesised enantioselectively by employing the Sharpless asymmetric epoxidation reaction of the unsymmetrical divinylmethanol, as a key step.

Enantiocontrolled synthesis of (115,125,135)-(9z,15z)- and (11a,125,135)-(9z,15z)-11-hydroxy-12,13-epoxy octadecadienoic acids by means of the sharpless asymmetric epoxidation of the unsymmetrical divinylcarbinol

(115,125,135K9Z,15Z)- and (11R,12S,13SM9Z,15Z)-11-Hydroxy-12,13-epoxy octadecadienoic acids, self defensive substances against the rice blast disease, were synthesized enantioselectively by employing the Sharpless asymmetric epoxidation reaction of the unsymmetrical divinylcarbinol, as a key step.

Stereoselective synthesis of methyl (11S,12S,13S)-(9Z,15Z)-11-hydroxy-12,13-epoxy octadecadienoate from D-mannose

The title compound, a self defensive substance against the rice blast disease, was synthesized from D-mannose in ten steps. The key intermediate 6 was prepared with Grignard addition of lactol 5 in favoured anti-selectivity.