86450-74-0 Usage
Uses
Used in Medicinal Research:
[2S,(+)]-5-[2-(3-Furanyl)ethyl]-1,2,3,4,4a,7,8,8aα-octahydro-1,1,4aβ,6-tetramethylnaphthalene-2β-ol is used as a compound of interest in medicinal research for its potential to be developed into pharmaceutical agents. Its unique structure and chirality may offer novel interactions with biological targets, leading to the discovery of new therapeutic agents.
Used in Chemical Research:
In the field of chemical research, [2S,(+)]-5-[2-(3-Furanyl)ethyl]-1,2,3,4,4a,7,8,8aα-octahydro-1,1,4aβ,6-tetramethylnaphthalene-2β-ol serves as a subject for studying the effects of stereochemistry and structural complexity on chemical reactivity and stability. Its properties may provide insights into the development of new synthetic pathways and the understanding of molecular interactions.
Used in Pharmaceutical Development:
[2S,(+)]-5-[2-(3-Furanyl)ethyl]-1,2,3,4,4a,7,8,8aα-octahydro-1,1,4aβ,6-tetramethylnaphthalene-2β-ol is utilized as a starting material or intermediate in the synthesis of pharmaceutical compounds. Its unique structural features may be leveraged to create new drugs with improved efficacy and selectivity.
Used in Chiral Chemistry:
In chiral chemistry, [2S,(+)]-5-[2-(3-Furanyl)ethyl]-1,2,3,4,4a,7,8,8aα-octahydro-1,1,4aβ,6-tetramethylnaphthalene-2β-ol is used as a model compound to study the effects of chirality on chemical reactions and to develop methods for the synthesis of enantiomerically pure compounds. Its (2S) configuration may be particularly relevant for understanding stereoselective processes in organic synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 86450-74-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,4,5 and 0 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 86450-74:
(7*8)+(6*6)+(5*4)+(4*5)+(3*0)+(2*7)+(1*4)=150
150 % 10 = 0
So 86450-74-0 is a valid CAS Registry Number.
86450-74-0Relevant academic research and scientific papers
SYNTHESIS OF (+)-BAIYUNOL, THE DITERPENE AGLYCONE OF THE SWEET GLYCOSIDE BAIYUNOSIDE
Mori, Kenji,Komatsu, Makoto
, p. 3409 - 3412 (2007/10/02)
A chiral synthesis of (+)-baiyunol, the labdane-type diterpene aglycone of the sweet glycoside baiyunoside, was achieved starting from (S)-3-hydroxy-2,2-dimethylcyclohexanone.
