95263-32-4 Usage
Uses
Used in Medicinal Chemistry:
(11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol is used as a compound of interest in medicinal chemistry for its potential to interact with biological targets due to its hydroxyl groups and cyclic structure. The presence of multiple hydroxyl groups may allow for hydrogen bonding, which is crucial for molecular recognition and binding processes.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (11aR)-1,1-dimethyl-8-(propan-2-yl)-1,2,3,4,5,10,11,11a-octahydro-4aH-dibenzo[a,d][7]annulene-4a,5,7-triol may be utilized as a starting material or a structural component in the design of new drugs. Its unique structural features could be leveraged to create molecules with specific therapeutic effects, targeting a range of diseases or conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 95263-32-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,2,6 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95263-32:
(7*9)+(6*5)+(5*2)+(4*6)+(3*3)+(2*3)+(1*2)=144
144 % 10 = 4
So 95263-32-4 is a valid CAS Registry Number.
95263-32-4Relevant academic research and scientific papers
Hasegawa, Shinichi,Kojima, Toshimi,Hirose, Yoshiyuki
, p. 1545 - 1552 (1985)
Key Word Index - Chamaecyparis pisifera; Cupressaceae; chemotaxonomy; mono-, sesqui- and diterpenes; 20-nor-abietane; 9(10 -> 20)-abeo-abietane. - Six new diterpenes, 12-hydroxy-20-nor-abieta-1(10),2,8,11,13-pentaene, pisiferanol (10S,12-dihydroxy-9(10 -> 20)-abeo-abieta-8,11,13-triene), pisiferadinol (20S-hydroxypisiferanol), 12-deoxypisiferanol, 1β-hydroxyisopisiferin (1R,12-dihydroxy-9(10 -> 20)-abeo-abieta-8,10(20),11,13-tetraene), and the dimethylamine salt of O-methylpisiferic acid were isolated from the seed of Chamaecyparis pisifera.The structures of these diterpenes were established by spectral and chemical methods.In addition, 15 mono-, four sesqui- and nine diterpenes were identified.