463-24-1 Usage
Uses
Used in Organic Chemistry:
9-Fluoro-1-nonanol is used as a synthetic intermediate for the preparation of various organic compounds. Its unique fluorinated structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
9-Fluoro-1-nonanol is used as a building block in the synthesis of pharmaceutical compounds. Its incorporation into drug molecules can enhance their properties, such as solubility, stability, and bioavailability, leading to improved therapeutic effects.
Used in Material Science:
9-Fluoro-1-nonanol is used as a component in the development of new materials with specific properties. Its fluorinated nature can contribute to the creation of materials with enhanced chemical resistance, thermal stability, and other desirable characteristics.
Used in Environmental Protection:
9-Fluoro-1-nonanol is used in the formulation of environmentally friendly products, such as biodegradable plastics and coatings. Its incorporation can improve the sustainability and eco-friendliness of these materials, reducing their environmental impact.
Used in Research and Development:
9-Fluoro-1-nonanol is used as a research compound in academic and industrial laboratories. Its unique properties make it a valuable tool for studying chemical reactions, exploring new synthesis methods, and developing innovative applications.
Check Digit Verification of cas no
The CAS Registry Mumber 463-24-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 463-24:
(5*4)+(4*6)+(3*3)+(2*2)+(1*4)=61
61 % 10 = 1
So 463-24-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H19FO/c10-8-6-4-2-1-3-5-7-9-11/h11H,1-9H2
463-24-1Relevant academic research and scientific papers
Tremblay, Amy E.,Buist, Peter H.,Hodgson, Derek,Dawson, Brian,Whittle, Ed,Shanklin, John
, p. 629 - 632 (2006)
1H-decoupled 19F NMR has been used to monitor the highly regioselective oxidation of a fluorine-tagged thia-fatty acid derivative by castor stearoyl-ACP Δ9 desaturase. The major enzymatic product, after reductive work-up, was identified as 9-fluoro-1-nonanol. This compound could be easily distinguished from substrate and a 9-sulfoxy by-product on the basis of its 19F NMR chemical shift and spiking experiments using authentic standards. Structural assignment of the cleavage product was confirmed by GC-MS analysis of the enzymatic products. Copyright
