72567-24-9 Usage
General Description
2,4-diphenyl-3,4,4a,5,6,7,8,8a-octahydro-2H-chromene is a chemical compound that belongs to the group of octahydro-2H-chromene derivatives. It is a bicyclic compound consisting of a benzene ring and a tetrahydro-2H-chromene ring structure. 2,4-diphenyl-3,4,4a,5,6,7,8,8a-octahydro-2H-chromene is used in various pharmaceutical and medicinal applications due to its potential biological activities such as antitumor, antiviral, and anti-inflammatory properties. Its chemical structure and properties make it a promising candidate for drug development and research in the field of medicinal chemistry.
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 articles and documents
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