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CAS 13956-51-9

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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-,(3R,4S,4aR,6aS,9aR,11R,13aR,13bS,15aS,15bR)-

Description:
1H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol, with the CAS number 13956-51-9, 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 (3R,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. Its intricate structure may impart unique physical properties, such as high melting and boiling points, and it may exhibit interesting optical properties due to its chirality. Additionally, the compound's potential applications could span fields such as organic synthesis, materials science, and medicinal chemistry, although specific uses would depend on further research into its biological activity and stability. Overall, this compound represents a fascinating example of complex organic chemistry with potential implications in various scientific domains.
Formula:C30H50O3
Synonyms:
  • C(14a)-Homo-27-norgammacer-14-ene-3a,21b,24-triol (8CI)
  • Lycoclavanol (7CI)
  • 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-,[3R-(3a,4b,4aa,6ab,9ab,11a,13aa,13bb,15aa,15bb)]-
  • C(14a)-Homo-27-norgammacer-14-ene-3,21,23-triol, (3a,4b,21b)-
  • Serrat-14-en-3a,21b,24-triol
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