60451-92-5 Usage
Uses
Used in Biochemical Research:
17-IODOHEPTADECANOIC ACID is used as a biochemical tool for studying lipid metabolism. Its unique structure allows researchers to investigate the role of fatty acids in various biological processes.
Used in Pharmaceutical Synthesis:
17-IODOHEPTADECANOIC ACID is used as a precursor for the synthesis of various pharmaceuticals and organic compounds. Its versatile chemical properties make it a valuable building block in the development of new drugs and therapeutic agents.
Used in Antimicrobial Applications:
17-IODOHEPTADECANOIC ACID has been studied for its potential antibacterial and antifungal properties. Its iodine atom may contribute to its effectiveness in inhibiting the growth of harmful microorganisms, making it a candidate for use in antimicrobial treatments.
Used in Chemical Industry:
17-IODOHEPTADECANOIC ACID is used in the chemical industry for the synthesis of various organic compounds. Its long-chain structure and functional groups make it a useful intermediate in the production of specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 60451-92-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,5 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60451-92:
(7*6)+(6*0)+(5*4)+(4*5)+(3*1)+(2*9)+(1*2)=105
105 % 10 = 5
So 60451-92-5 is a valid CAS Registry Number.
InChI:InChI=1/C17H33IO2/c18-16-14-12-10-8-6-4-2-1-3-5-7-9-11-13-15-17(19)20/h1-16H2,(H,19,20)
60451-92-5Relevant academic research and scientific papers
Acides gras marques en position ω par un nucleide radioactif emetteur γ
Riche, Francoise,Mathieu, Jean-Paul,Vincens, Maurice,Bardy, Andre,Comet, Michel,Vidal, Michel
, p. 49 - 55 (2007/10/02)
The synthesis of many saturated, acetylenic, olefinic (Z or E) fatty acids labeled with 123I or 131I at the ω-position has been achieved.The radioactive iodine atom is introduced by a I-, *I- exchange reaction; the influence on the yield of several parameters - presence of iodine carrier, fatty acid and water concentrations, solution acidity - has been studied.Experimental conditions which produce labeling yields higher than 95percent have been defined; these results have lead to a very easy labeling method used in several hospitals in the external study of myocardial metabolism of fatty acids.
