72567-24-9 Usage
Uses
Used in Pharmaceutical and Medicinal Applications:
2,4-diphenyl-3,4,4a,5,6,7,8,8a-octahydro-2H-chromene is utilized as a pharmaceutical agent for its antitumor, antiviral, and anti-inflammatory properties. Its unique chemical structure and biological activities contribute to its potential in developing new drugs for treating various diseases and conditions.
Used in Drug Development:
In the field of medicinal chemistry, 2,4-diphenyl-3,4,4a,5,6,7,8,8a-octahydro-2H-chromene serves as a key compound for drug development. Its properties and structure make it a valuable asset in the discovery and design of new therapeutic agents with improved efficacy and safety profiles.
Used in Research:
2,4-diphenyl-3,4,4a,5,6,7,8,8a-octahydro-2H-chromene is also employed as a research tool in medicinal chemistry. It aids scientists in understanding the mechanisms of action, structure-activity relationships, and potential applications of octahydro-2H-chromene derivatives in therapeutic interventions.
Check Digit Verification of cas no
The CAS Registry Mumber 72567-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,5,6 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72567-24:
(7*7)+(6*2)+(5*5)+(4*6)+(3*7)+(2*2)+(1*4)=139
139 % 10 = 9
So 72567-24-9 is a valid CAS Registry Number.
InChI:InChI=1/C21H24O/c1-3-9-16(10-4-1)19-15-21(17-11-5-2-6-12-17)22-20-14-8-7-13-18(19)20/h1-6,9-12,18-21H,7-8,13-15H2
72567-24-9Relevant academic research and scientific papers
SYNTHESIS AND CATALYTIC HYDROGENATION OF 5-OXOTETRAHYDRO-4H-CHROMENES
Kharchenko, V. G.,Markova, L. I.,Smirnova, N. S.,Korshunova, K. M.,Rybina, G. I.
, p. 1926 - 1930 (2007/10/02)
A systematic investigation was undertaken into the intramolecular heterocyclization of 2-(3-oxopropyl)-1,3-cyclohexanediones by the action of chemical reagents.It was established that the direction of the heterocyclization reactions depends on the structure of the initial compound, the temperature, and the cyclizing agent.It was shown that the investigated compounds can undergo cyclization with the formation of 5-oxo-5,6,7,8-tetrahydro-4H-chromenes, which are capable of being converted into hexahydrochromans and 5-oxo-1-oxabicyclodec-9-enes under the conditions of catalytic hydrogenation.
CHARACTER OF THE TRANSFORMATIONS OF 2-(3-OXOALKYL)-1-CYCLOHEXANONES AND 1,3-CYCLOHEXANEDIONES
Kharchenko, V. G.,Smirnova, N. S.,Markova, L. I.,Vlasova, L. V.,Rybina, G. I.,Korshunova, K.M.
, p. 700 - 702 (2007/10/02)
2-(3-Oxoalkyl)-1-cyclohexanones and 1,3-cyclohexanediones undergo cyclization under the conditions of catalytic hydrogenation over rhodium and copper-chromium catalysts to form hexahydrochromans.The possibility of hydrogenation of aryl substituents to cyc
