2724-59-6 Usage
Description
17-METHYLOCTADECANOIC ACID, also known as 17-methyl stearic acid, is a branched-chain saturated fatty acid derived from octadecanoic (stearic) acid with a methyl substituent at position 17. It has been identified in various natural sources such as murine meibomian glands, C. cornucopioides mushrooms, Phyllobacterium species, and the aerial parts of C. ladanifer, where its concentration varies seasonally.
Uses
Used in Pharmaceutical Industry:
17-METHYLOCTADECANOIC ACID is used as a potential therapeutic agent for various medical applications due to its unique chemical structure and presence in different biological sources. Its specific role and application in the pharmaceutical industry may vary based on further research and development.
Used in Cosmetic Industry:
In the cosmetic industry, 17-METHYLOCTADECANOIC ACID may be utilized as an ingredient in the formulation of skincare and personal care products, capitalizing on its fatty acid properties to provide moisturization and improve skin health.
Used in Chemical Research:
17-METHYLOCTADECANOIC ACID serves as a subject of interest in chemical research, where its unique structure and natural occurrence can be explored for potential applications in the development of new compounds or materials.
Used in Agricultural Industry:
The agricultural industry may benefit from the study of 17-METHYLOCTADECANOIC ACID, particularly in understanding its role in the growth and development of certain plant species, which could lead to improvements in crop yield and resistance to diseases.
Please note that the specific applications and reasons for using 17-METHYLOCTADECANOIC ACID may vary depending on the industry and the results of ongoing research. The provided uses are based on the general properties of the compound and its natural occurrence in various sources.
Check Digit Verification of cas no
The CAS Registry Mumber 2724-59-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,2 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2724-59:
(6*2)+(5*7)+(4*2)+(3*4)+(2*5)+(1*9)=86
86 % 10 = 6
So 2724-59-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H38O2/c1-18(2)16-14-12-10-8-6-4-3-5-7-9-11-13-15-17-19(20)21/h18H,3-17H2,1-2H3,(H,20,21)
2724-59-6Relevant articles and documents
A practical synthesis of long-chain iso-fatty acids (iso-C 12-C19) and related natural products
Richardson, Mark B.,Williams, Spencer J.
supporting information, p. 1807 - 1812 (2013/10/22)
A gram-scale synthesis of terminally-branched iso-fatty acids (iso-C 12-C19) was developed commencing with methyl undec-10-enoate (methyl undecylenate) (for iso-C12-C14) or the C15 and C16 lactones pentadecanolide (for iso-C 15-C17) and hexadecanolide (for iso-C18-C 19). Central to the approaches outlined is the two-step construction of the terminal isopropyl group through addition of methylmagnesium bromide to the ester/lactones and selective reduction of the resulting tertiary alcohols. Thus, the C12, C17 and C18 iso-fatty acids were obtained in three steps from commercially-available starting materials, and the remaining C13-C16 and C19 iso-fatty acids were prepared by homologation or recursive dehomologations of these fatty acids or through intercepting appropriate intermediates. Highlighting the synthetic potential of the iso-fatty acids and various intermediates prepared herein, we describe the synthesis of the natural products (S)-2,15-dimethylpalmitic acid, (S)-2-hydroxy-15-methylpalmitic acid, and 2-oxo-14-methylpentadecane.
Dilithium tetrachlorocuprate catalyzed alkylation of aleuritic acid derivatives and synthesis of muscalure
Subramanian,Ahuja, Seema
, p. 724 - 726 (2007/10/03)
Carbon-carbon coupling with the ω-halo or tosyl derivatives of threo-9,10,16-trihydroxyhexadecanoic acid (aleuritic acid) has been carried out in the presence of dilithium tetrachlorocuprate reagent and a short synthesis of muscalure is reported.
