24613-65-8 Usage
Uses
1. Used in Antiviral and Anticancer Research:
1,9-DIIODONONANE is used as a chemical modifier for the optimization studies of DNA-binding marine natural products, such as aaptamine. Its presence in these studies aids in enhancing the antiviral and anticancer properties of the compounds, making them more effective against various diseases.
2. Used in Pharmaceutical Industry:
1,9-DIIODONONANE can be utilized in the development of new drugs and therapies, particularly in the areas of antiviral and anticancer treatments. Its unique chemical structure allows for potential interactions with biological targets, making it a valuable compound for pharmaceutical research and development.
3. Used in Chemical Synthesis:
Due to its distinct structure, 1,9-DIIODONONANE can be employed as a starting material or intermediate in the synthesis of various organic compounds. Its iodine atoms can be used for further functionalization, leading to the creation of new molecules with potential applications in different industries.
4. Used in Analytical Chemistry:
1,9-DIIODONONANE can be utilized as a reference compound or standard in analytical chemistry, particularly in techniques involving chromatography and mass spectrometry. Its unique properties make it suitable for calibrating instruments and validating analytical methods.
Check Digit Verification of cas no
The CAS Registry Mumber 24613-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24613-65:
(7*2)+(6*4)+(5*6)+(4*1)+(3*3)+(2*6)+(1*5)=98
98 % 10 = 8
So 24613-65-8 is a valid CAS Registry Number.
InChI:InChI=1/C9H18I2/c10-8-6-4-2-1-3-5-7-9-11/h1-9H2
24613-65-8Relevant academic research and scientific papers
Highly Selective Radical Monoreduction of Dihalides Confined to a Dynamic Supramolecular Host
Petroselli, Manuel,Rebek, Julius,Yu, Yang
supporting information, p. 3284 - 3287 (2021/02/05)
Reduction of alkyl dihalide guests (2–5 and 7) with trialkylsilanes (R3SiH) was performed in water-soluble host 1 to investigate the effects of confinement on fast radical reactions (k≥103 m?1 s?1). High selectivity (>95 %) for mono-reduced products was observed for primary and secondary dihalide guests under mild conditions. The results highlight the importance of host–guest complexation rates to modulate the product selectivity in radical reactions.
Radical Reactions in Cavitands Unveil the Effects of Affinity on Dynamic Supramolecular Systems
Angamuthu, Venkatachalam,Petroselli, Manuel,Rahman, Faiz-Ur,Rebek, Julius,Yu, Yang,Zhao, Xinluo
supporting information, (2020/02/18)
Radical reduction of alkyl halides and aerobic oxidation of alkyl aromatics are reported using water-soluble container compounds (1 and 2). The reductions involve α,ω-dihalides (4-8 and 10) with radical initiators in cavitand hosts with varied binding affinities. Product distributions lead to general guidelines for the use of dynamic supramolecular systems with fast reactions. The binding of guest substrates in the hosts must show high affinities (Ka> 103M-1) to ensure that the reactions take place under confinement in the containers.
