67529-83-3

Upstream product

• 67-56-1 methanol 
• 141-22-0 Ricinoleic acid 
• 111-71-7 heptanal 
• 111-81-9 Methyl 10-undecenoate 

Downstream Products

• 36971-14-9 dec-1-en-4-ol 
• 25601-41-6 methyl 9-decenoate 
• 6114-39-2 methyl 12-hydroxyoctadecanoate 
• 1842-70-2 methyl 9-oxooctadecanoate 
• 112-61-8 Methyl stearate 
• 822-10-6 octadeca-9,11-dienoic acid methyl ester 
• 822-10-6 (9Z,11E)-methyl octadeca-9,11-dienoate 
• 10038-16-1 methyl 8-(5-hexyl-2-furyl)-octanoate 
• 13481-97-5 dimethyl 9-octadecen-1,18-dioate 
• 1383325-22-1 methyl 12-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]octadec-9-enoate 
• 822-10-6 methyl cis,cis-9,11-octadecadienoate 
• 112-63-0 Methyl linoleate 
• 111-81-9 Methyl 10-undecenoate 
• 106-14-9 12-Hydroxystearic acid 

Relevant academic research and scientific papers

[1 + 1]-Condensation of 12-Oxo-Derivatives of Ricinoleic Acid Esters with Hydrazine Hydrate on the Route to Macrocycles

The reactivities of the keto analogs of methyl ricinolate and its triglyceride with hydrazine hydrate were studied. The ester was found to be inert, which made it possible to synthesize a macrocyclic azine with a side chain hydrazone moiety from a 12-oxo-derivative.

Synthesis of enantiomerically pure 2,3,4,6-tetrasubstituted tetrahydropyrans by Prins-type cyclization of methyl ricinoleate and aldehydes

The AlCl3-catalyzed Prins-type cyclization of methyl ricinoleate (1), an enantiomerically pure renewable compound, with aldehydes such as heptanal (2a), isobutyraldehyde (2b), pivaldehyde (2c) and benzaldehyde (2d) is a simple reaction for the diastereoselective synthesis of enantiomerically pure 2,3,6-trialkyl-substituted 4-chlorotetrahydropyrans. The respective 4-hydroxytetrahydropyrans are obtained e.g. with aldehydes 2a and 2d using montmorillonite KSF/O as the catalyst. Wiley-VCH Verlag GmbH & Co. KGaA, 2006.