65520-48-1 Usage
General Description
1,2:13,14-Diepoxytetradecane is a chemical compound with the molecular formula C14H28O2. It is a type of epoxide compound, which means it contains an oxygen atom bonded to two adjacent carbon atoms. This particular compound has two epoxide groups, which are highly reactive and can undergo chemical reactions with a variety of other compounds. 1,2:13,14-Diepoxytetradecane is commonly used in organic synthesis and as a chemical intermediate for manufacturing other compounds. It is important to handle this compound with caution, as it can be harmful if inhaled, ingested, or absorbed through the skin, and it may also be a skin and eye irritant. Proper safety precautions should be taken when handling and using 1,2:13,14-Diepoxytetradecane.
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 articles and documents
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
