CAS 24513-57-3
:1H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol,2,3,4,4a,5,6,6a,7,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-eicosahydro-4-(hydroxymethyl)-4,6a,10,10,13a,15b-hexamethyl-,(3S,4S,4aR,6aS,9aR,11R,13aR,13bS,15aS,15bR)- (9CI)
Description:
1H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol, with the CAS number 24513-57-3, is a complex organic compound characterized by its polycyclic structure, which consists of fused naphthalene rings and a cycloheptane moiety. This compound features multiple stereocenters, contributing to its chiral nature, and exhibits specific stereochemistry denoted by its (3S,4S,4aR,6aS,9aR,11R,13aR,13bS,15aS,15bR) configuration. The presence of hydroxymethyl groups at specific positions enhances its reactivity and solubility in various solvents. As a member of the larger class of polycyclic aromatic hydrocarbons, it may exhibit interesting electronic properties and potential applications in materials science or medicinal chemistry. Its structural complexity suggests potential for diverse interactions in biological systems, although specific biological activity would require further investigation. Overall, this compound represents a unique example of synthetic organic chemistry with implications for research in various fields.
Formula:C30H50O3
Synonyms:- C(14a)-Homo-27-norgammacer-14-ene-3,21,24-triol,(3b,4b,21b)-
- C(14a)-Homo-27-norgammacer-14-ene-3b,21b,24-triol (8CI)
- 1H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol,2,3,4,4a,5,6,6a,7,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-eicosahydro-4-(hydroxymethyl)-4,6a,10,10,13a,15b-hexamethyl-,[3S-(3a,4a,4ab,6aa,9aa,11a,13ab,13ba,15ab,15ba)]-
- 21-Episerratriol
- 3-Epilycoclavanol
- Serrat-14-en-3b,21b,24-triol
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Found 3 products.
21-Episerratriol
CAS:<p>21-Episerratriol is a natural product of Lycopodium, Lycopodiaceae.</p>Formula:C30H50O3Purity:98%Color and Shape:SolidMolecular weight:458.7221-Episerratriol
CAS:Controlled Product<p>21-Episerratriol is a triterpenoid compound, which is a type of chemical product characterized by a structure based on five isoprene units. It is derived from natural sources, particularly from certain plant species known for their diverse phytochemical profiles. The mode of action of 21-Episerratriol involves interacting with various biological pathways, potentially influencing metabolic and signaling processes within cells. This interaction suggests its role in modulating enzymatic activities and cellular responses, making it a compound of interest in pharmacological and biochemical research.</p>Formula:C30H50O3Purity:Min. 95%Molecular weight:458.7 g/mol


