28393-06-8 Usage
Uses
Used in Pharmaceutical Applications:
10,12-Heptadecadiynoic acid is used as a pharmaceutical agent for its potential anti-inflammatory and anti-microbial properties, making it a candidate for the development of new treatments for various inflammatory and infectious diseases.
Used in Cancer Research:
In cancer research, 10,12-heptadecadiynoic acid is used as an agent to inhibit the growth of cancer cells, offering a potential therapeutic approach for cancer treatment.
Used in Electronic Devices:
10,12-Heptadecadiynoic acid is used in the development of electronic devices due to its unique electronic properties, which may contribute to advancements in areas such as semiconductors and electronic components.
Used in Optical Devices:
In the field of optics, 10,12-heptadecadiynoic acid is utilized for its optical properties, potentially leading to innovations in optical communication and sensing technologies.
Used in Research:
10,12-Heptadecadiynoic acid serves as a valuable research tool for studying the structure and function of fatty acids, as well as their interactions with biological systems and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 28393-06-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,3,9 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28393-06:
(7*2)+(6*8)+(5*3)+(4*9)+(3*3)+(2*0)+(1*6)=128
128 % 10 = 8
So 28393-06-8 is a valid CAS Registry Number.
InChI:InChI=1/C17H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19/h2-4,9-16H2,1H3,(H,18,19)
28393-06-8Relevant academic research and scientific papers
Synthesis and Nuclear Magnetic Resonance Studies on a Series of Synthesis Long-chain Tellurophene Fatty Esters
Jie, Marcel S. F. Lie Ken,Chau, Sherman H.
, p. 2642 - 2657 (2007/10/03)
The synthesis and the results of the 1H and 13C NMR spectroscopic analyses of thirteen 2,5-disubstituted tellurophene fatty esters, containing substituents of different chain lengths, and of a monosubstituted tellurophene ester are repported.The tellurophene esters are obtained by cyclization of the corresponding conjugated intermediates with Na2Te in the presence of AgOAc in methanol.The tellurophene moiety in the alkyl chain induces a deshielding effect on the protons of the adjacent methylene prtons.The shift parameters of the tellurophene moiety on the shifts of the adjacent methylene carbon atoms are also determined.
