53704-25-9 Usage
Uses
Used in Pharmaceutical Industry:
(2E)-2-[(2E)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE is used as a potential pharmaceutical compound for its possible biological activities and therapeutic effects. Its specific uses and properties in this industry would need to be further studied and determined.
Used in Research:
(2E)-2-[(2E)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE serves as a subject of research for scientists and researchers interested in exploring its chemical properties, potential reactions, and applications in various fields. Further studies would be required to understand its full potential and possible uses.
Used in Other Industries:
(2E)-2-[(2E)-2-(1,3,3-TRIMETHYL-1,3-DIHYDRO-2H-INDOL-2-YLIDENE)ETHYLIDENE]-3,4-DIHYDRONAPHTHALEN-1(2H)-ONE may also have potential applications in other industries, such as materials science or chemical manufacturing. However, its specific uses and properties in these industries would need to be further studied and determined.
Check Digit Verification of cas no
The CAS Registry Mumber 53704-25-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,7,0 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 53704-25:
(7*5)+(6*3)+(5*7)+(4*0)+(3*4)+(2*2)+(1*5)=109
109 % 10 = 9
So 53704-25-9 is a valid CAS Registry Number.
InChI:InChI=1/C23H23NO/c1-23(2)19-10-6-7-11-20(19)24(3)21(23)15-14-17-13-12-16-8-4-5-9-18(16)22(17)25/h4-11,14-15H,12-13H2,1-3H3/b17-14+,21-15+
53704-25-9Relevant academic research and scientific papers
EFFECT OF THE INCLUSION OF A CYCLIC FRAGMENT IN THE CHROMOPHORE ON THE PROPERTIES OF A SPIROPYRAN-MEROCYANINE SYSTEM
Gal'bershtam, M. A.,Sidorov, A. P.,Przhiyalgovskaya, N. M.,Strokach, Yu. P.,Barachevskii, V. A.,et. al.
, p. 923 - 928 (2007/10/02)
The corresponding merocyanines, which do not display a tendency to form spiropyran structures, are formed in the condensation of 1,3,3-trimethyl-2-methyleneindoline with 5-methyl-2-furoylacetaldehyde, 2-formylcyclohexanone, or 2-formyl-1-tetralone.Spiran compounds in which the spiropyran-merocyanine equilibrium is shifted markedly to favor the closed form are formed when 4a,9-dimethyl-2,3,4,4a-tetrahydrocarbazone - the cyclic analog of the Fischer base - is used in the reaction with salicylaldehydes and benzoylacetaldehydes.
