65520-48-1 Usage
Uses
Used in Organic Synthesis:
1,2:13,14-Diepoxytetradecane is used as a reactive intermediate in organic synthesis for its ability to participate in a range of chemical reactions, facilitating the creation of diverse organic compounds.
Used in Chemical Intermediates Production:
In the chemical industry, 1,2:13,14-Diepoxytetradecane is utilized as a chemical intermediate, playing a pivotal role in the synthesis of other complex compounds, which may have various applications in different fields.
Used in Research and Development:
Due to its unique reactivity, 1,2:13,14-Diepoxytetradecane is employed in research and development settings to explore new chemical pathways and develop innovative materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 65520-48-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 65520-48:
(7*6)+(6*5)+(5*5)+(4*2)+(3*0)+(2*4)+(1*8)=121
121 % 10 = 1
So 65520-48-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O2/c1(3-5-7-9-13-11-15-13)2-4-6-8-10-14-12-16-14/h13-14H,1-12H2
65520-48-1Relevant academic research and scientific papers
Synthesis of linear aza and thio analogues of acetogenins and evaluation of their cytotoxicity
Villo, Piret,Toom, Lauri,Eriste, Elo,Vares, Lauri
, p. 6886 - 6899 (2013/11/06)
We report the stereoselective synthesis of thio and aza analogues of Annonaceous acetogenins. The synthetic route allows easy variation of the stereochemistry and of the thio- and aza-fragments. Kinetic resolution of terminal bis-epoxides was used to set two remote stereocentres with high enantio- and diastereoselectivities in one step. The cytotoxicity of the analogues was assessed using the HeLa cell line. Four aza and two thio analogues of Annonaceous acetogenins were synthesized according to a general synthetic route. Two remote stereocentres in the analogues were set with high enantio- and diastereoselectivity in one step by hydrolytic kinetic resolution of a terminal bis-epoxide. Copyright
