28267-29-0 Usage
Description
ETHYL TRIDECANOATE, also known as Tridecanoic acid Ethyl ester, is a fatty acid ester that belongs to the Ethyl Esters category. It is the ethyl ester of Tridecanoic Acid, which is commonly found in dairy products and is used to synthesize Testosterone Tridecanoate. Ethyl tridecanoate is a natural product found in various plants, including Saussurea involucrata, Houttuynia cordata, and Houttuynia.
Uses
Used in Pharmaceutical Industry:
ETHYL TRIDECANOATE is used as a synthetic compound for the production of Testosterone Tridecanoate, which is utilized in the pharmaceutical industry for hormone replacement therapy and the treatment of various medical conditions related to testosterone deficiency.
Used in Food Industry:
ETHYL TRIDECANOATE is used as a flavoring agent for enhancing the taste and aroma of certain food products, taking advantage of its natural occurrence in dairy products.
Used in Chemical Research:
ETHYL TRIDECANOATE is used as a research compound in the field of organic chemistry, particularly for studying the properties and reactions of fatty acid esters and their potential applications in various chemical processes.
Used in Perfumery:
ETHYL TRIDECANOATE is used as a fragrance ingredient in the perfumery industry, contributing to the creation of unique and complex scents in perfumes and other fragrance products.
Synthesis Reference(s)
Tetrahedron Letters, 32, p. 3091, 1991 DOI: 10.1016/0040-4039(91)80697-5
Check Digit Verification of cas no
The CAS Registry Mumber 28267-29-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,6 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 28267-29:
(7*2)+(6*8)+(5*2)+(4*6)+(3*7)+(2*2)+(1*9)=130
130 % 10 = 0
So 28267-29-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H30O2/c1-3-5-6-7-8-9-10-11-12-13-14-15(16)17-4-2/h3-14H2,1-2H3
28267-29-0Relevant articles and documents
Suzuki-miyaura cross-coupling reactions of unactivated alkyl halides catalyzed by a nickel pincer complex
Di Franco, Thomas,Boutin, Nicolas,Hu, Xile
, p. 2949 - 2958 (2013/11/06)
A nickel(II) pincer complex, [(MeN2N)Ni-Cl], was used to catalyze alkyl-alkyl and alkyl-aryl Suzuki-Miyaura coupling reactions of unactivated alkyl halides. The coupling of 9-alkyl-9-borabicyclo[3.3.1]nonane and 9-phenyl-9-borabicyclo[3.3.1]nonane reagents with alkyl halides was achieved in modest to good yields. The reactions tolerated a variety of useful functional groups including ester, ether, furan, thioether, acetal, and Boc groups. Georg Thieme Verlag Stuttgart, New York.
Cobalt-catalyzed reductive coupling of saturated alkyl halides with activated alkenes
Shukla, Paritosh,Hsu, Yun-Chu,Cheng, Chien-Hong
, p. 655 - 658 (2007/10/03)
An efficient cobalt-catalyzed reductive coupling reaction of alkyl halides with electron-withdrawing alkenes (CH2=CR1EWG, EWG = electron-withdrawing group) in the presence of water and zinc powder in acetonitrile to give the corresponding Michael-type addition product (RCH 2CR1EWG) was described. The methodology is versatile such that unactivated primary, secondary, and tertiary alkyl bromides and iodides and various conjugated alkenes including acrylates, acrylonitrile, methyl vinyl ketone, and vinyl sulfone all successfully participate in this coupling reaction. For the alkyl halides used in the reaction, the iodides generally gave heller yields compared to those of the corresponding bromides. It is a unique method employing CoI2dppe, zinc, and alkyl halides, affording conjugate addition products in high yields. Mechanistically, the reaction appears to follow an oxidative addition driven route rather than the previously reported radical route.
