99152-14-4 Usage
Description
[4aS,(+)]-1,2,3,4,5,10,11,11aα-Octahydro-1,1-dimethyl-8-(1-methylethyl)-4aH-dibenzo[a,d]cycloheptene-4aβ,7-diol is a complex organic compound belonging to the dibenzocycloheptene class. It features a seven-membered ring fused to two benzene rings, with a hydroxyl group at the 4aβ and 7 positions, and a methyl and isopropyl group at the 1 and 8 positions, respectively. The stereochemistry of the compound is indicated by [4aS,(+)], which describes the arrangement of substituents around the seven-membered ring. [4aS,(+)]-1,2,3,4,5,10,11,11aα-Octahydro-1,1-dimethyl-8-(1-methylethyl)-4aH-dibenzo[a,d]cycloheptene-4aβ,7-diol holds potential for various pharmacological and biological applications, making it a subject of interest for further research and possible use in the pharmaceutical and other industries.
Uses
Used in Pharmaceutical Industry:
[4aS,(+)]-1,2,3,4,5,10,11,11aα-Octahydro-1,1-dimethyl-8-(1-methylethyl)-4aH-dibenzo[a,d]cycloheptene-4aβ,7-diol is used as a potential pharmaceutical compound for its possible pharmacological and biological properties. Its unique chemical structure and stereochemistry make it a candidate for further study and development in the creation of new drugs or therapies.
Used in Chemical Research:
In the field of chemical research, [4aS,(+)]-1,2,3,4,5,10,11,11aα-Octahydro-1,1-dimethyl-8-(1-methylethyl)-4aH-dibenzo[a,d]cycloheptene-4aβ,7-diol serves as a subject for investigation into its chemical behavior, reactivity, and potential interactions with other compounds. Understanding these properties can lead to new insights and applications in various chemical processes and industries.
Used in Material Science:
[4aS,(+)]-1,2,3,4,5,10,11,11aα-Octahydro-1,1-dimethyl-8-(1-methylethyl)-4aH-dibenzo[a,d]cycloheptene-4aβ,7-diol's unique structure and properties may also find applications in material science, where it could be studied for potential uses in the development of new materials with specific characteristics, such as improved strength, flexibility, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 99152-14-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,1,5 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99152-14:
(7*9)+(6*9)+(5*1)+(4*5)+(3*2)+(2*1)+(1*4)=154
154 % 10 = 4
So 99152-14-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H30O2/c1-13(2)16-10-14-6-7-18-19(3,4)8-5-9-20(18,22)12-15(14)11-17(16)21/h10-11,13,18,21-22H,5-9,12H2,1-4H3/t18-,20-/m0/s1
99152-14-4Relevant articles and documents
Semisynthesis of (-)-barbatusol, (+)-demethylsalvicanol, and (+)-rosmaridiphenol from (+)-pisiferic acid
Nisigaki, Eri,Sugamoto, Kazuhiro,Nishida, Misaki,Matsushita, Yoh-Ichi
, p. 746 - 748 (2016/07/16)
(+)-Pisiferic acid (1) was converted into (+)-12-O-methoxymethylpisiferol (5c) in 3 steps. The rearrangement of 5c with trifluoromethanesulfonic anhydride in pyridine provided (1)- 12-O-methoxymethylpisiferin (6c), which was converted into icetexane pheno
