7511-30-0

Usage

Uses

Used in Pharmaceutical Industry:
22-methoxy-22-oxodocosanoic acid is used as a therapeutic agent for the treatment of neurological disorders and metabolic diseases due to its unique chemical structure and potential biological activities. Its presence in natural fats and oils suggests that it may have roles in energy metabolism and cell membrane structure, which could be leveraged for therapeutic benefits.
Used in Research Applications:
In the field of scientific research, 22-methoxy-22-oxodocosanoic acid is used as a subject of study to explore its specific properties and potential biological activities. Further investigation into its physiological roles and therapeutic uses could lead to new insights and applications in medicine and healthcare.

Upstream product

• 22399-98-0 docosanedioic acid dimethyl ester 
• 67-56-1 methanol 
• 505-56-6 docosanedioic acid 
• 103168-13-4 10,13-dioxo-docos-11t-enedioic acid dimethyl ester 
• 14065-32-8 methyl 10-chloro-10-oxodecanoate 

Downstream Products

• 506-45-6 22-hydroxydocosanoic acid 
• 18060-84-9 22-hydroxy-tetracosanoic acid methyl ester 
• 18060-70-3 22-hydroxy-tetracosanoic acid 

Relevant academic research and scientific papers

Self-assembly of bolaamphiphiles forming alternating layer arrangements with lead and copper divalent ions

Five bifunctional ?±- amino acid-a??-carboxy bolaamphiphiles [(2-R,S, or RS)-(HOOC)-(CH2)m-CONH-(CH2)n-CH(COOH)(NH2 ) m = 20,22, n = 3,4 labeled (l), (d,l)-C22Orn (l), (d), (d,l)-C22Lys, (d,l)-C24Lys respectively] were synthesized. These molecules were deposited on different aqueous subphases, and studied by means of grazing incidence X-ray diffraction (GIXD). On deionized water, the bolaamphiphiles (d,l)-C22Lys yield a mixture of crystallites: both a monolayer, in which the chains are tilted from the normal, and a multilayer in which the molecules lie parallel to the water. On the other hand, when deposited on mono- or bi-metal ionic subphases, they self-assemble into crystalline multilayer films in which the molecules lie parallel to the aqueous solution surface, linked head-to-head and tail-to-tail in the form of extended chains. The latter are juxtaposed such that the metal ions form sheets separated by the organic molecules, aligned perpendicular to the plane of the aqueous solution. Deposition of either the enantiomerically pure or racemic bifunctional bolaamphiphiles on an aqueous solution of mixed Cu(Acetate)2 and Pb(Acetate)2, yields self-assembled crystalline films composed of the two different metal cations, arranged in alternating sheets, separated by the organic spacer. Both GIXD and X-ray-photoelectric-spectroscopy (XPS) studies (after deposition on solid support) demonstrate that the structures of these films differ form the ones formed on either pure Pb(Ac)2 or on Cu(Ac)2 solutions, thus excluding the simultaneous formation of the two monometallic crystalline phases.