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10,12-Octadecadienoic acid, 9-oxo-, methyl ester, (E,E)- is a chemical compound with the molecular formula C19H32O3. It is a type of unsaturated fatty acid ester, characterized by the presence of two double bonds (E,E) at the 10th and 12th carbon positions, and a keto group at the 9th carbon position. 10,12-Octadecadienoic acid, 9-oxo-, methyl ester, (E,E)- is derived from the methyl esterification of 9-oxo-10,12-octadecadienoic acid, which involves the reaction of the carboxylic acid group with methanol to form a methyl ester. It is commonly found in various natural sources, such as plants and microorganisms, and is known for its potential biological activities, including anti-inflammatory and antimicrobial properties. The compound's structure and properties make it a subject of interest in the fields of chemistry, biology, and medicine.

71201-23-5

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71201-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71201-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,2,0 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 71201-23:
(7*7)+(6*1)+(5*2)+(4*0)+(3*1)+(2*2)+(1*3)=75
75 % 10 = 5
So 71201-23-5 is a valid CAS Registry Number.

71201-23-5Downstream Products

71201-23-5Relevant academic research and scientific papers

Synthesis of the 9-oxo-diene derivative of methyl dimorphecolate by an efficient Oppenauer oxidation procedure

Tassignon, P.,Rijk, T. de,Wit, D. de,Buyck, L. de

, p. 39 - 42 (1994)

Oxidation of methyl dimorphecolate (1) to methyl 9-oxo-10,12-E,E-octadecadienoate (2) has been studied, using Oppenauer conditions. Acetone and cyclohexanone have been used as oxidizing ketones. Combination of cyclohexanone with inert solvents has been pe

Allylic oxidation: Easy synthesis of alkenones from activated alkenes with TEMPO

Breton, Tony,Liaigre, Denis,Belgsir, El Mustapha

, p. 2487 - 2490 (2007/10/03)

Activated alkenes and dienes are converted into the corresponding alkenone in excellent yields (>90%). In aqueous acetonitrile, the transformations are catalyzed by 2,2,6,6-tetramethyl-1-oxopiperidinium (TEMPO+) in the presence of water and 2,6-lutidine. TEMPO+ cations were regenerated electrochemically from the radical parent (TEMPO.) at a vitreous carbon anode.

New geometric isomers of oxooctadecadienoate in copper-catalyzed decomposition products of linoleate hydroperoxide

Tokita, Masako,Iwahara, Jyunko,Morita, Makio

, p. 993 - 997 (2007/10/03)

Methyl linoleate hydroperoxide produced by autoxidation was refluxed with 10-4 M Cu-naphthenate in benzene. Two new geometrical isomers of oxooctadecadienoate (compounds I and II) were found in addition to the four known isomers. They were isolated by a Sephadex LH-20 column chromatography with chloroform-hexane (2:1) and purified by HPLC on Nucleosil 100-5 and Zorbax ODS columns. UV, IR, MS, and 1H-NMR spectra were measured. The geometry of conjugated dienes were assigned from the coupling constants of the olefinic protons. Compounds I and II were identified as 13-oxo-trans-9, cis-11- and 9-oxo-cis-10, trans-12-octadecadienoate, respectively. Each of them had a cis double bond adjacent to the oxo group. The hydroperoxides of the same geometry as compounds I and II were also detected in autoxidation products.

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