15336-84-2 Usage
Chemical structure
A spirocyclic compound containing two epoxy groups and a diazaspiro ring.
Synonyms
DEC-732.
Potential applications
Multifunctional monomer for the synthesis of epoxy thermosets.
Thermal stability
Exhibits good thermal stability.
Mechanical properties
Demonstrates good mechanical properties.
Industrial applications
Adhesives, coatings, and composite materials.
Drug carrier potential
Has shown potential as a drug carrier.
Biocompatibility
Has potential in the development of biocompatible materials.
Check Digit Verification of cas no
The CAS Registry Mumber 15336-84-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,3 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 15336-84:
(7*1)+(6*5)+(5*3)+(4*3)+(3*6)+(2*8)+(1*4)=102
102 % 10 = 2
So 15336-84-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H20N2O4/c17-12-14(4-2-1-3-5-14)16(7-11-9-20-11)13(18)15(12)6-10-8-19-10/h10-11H,1-9H2
15336-84-2Relevant articles and documents
Investigation of the antitumor activity of new epoxide derivatives. II: N-glycidylated oxo-nitrogen heterocyles
Fischer,Moller,Budnowski,et al.
, p. 663 - 668 (2007/10/02)
A number of N-glycidyl compounds derived from oxo-substituted nitrogen heterocycles such as diazines, triazines, diazoles, triazoles as well as condensed ring systems containing these units have been synthesized. All products were tested for their antitumor activity against leukaemia in the mouse. Almost all of the approx. 50 di- and triglycidyl compounds showed activity and 5 of them exhibited an increase of lifespan of 200% and more. The most active compound was 1,2,4-triglycidyl-urazol.
