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CAS 1449-06-5

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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-4,4,6a,10,10,13a,15b-heptamethyl-,(3S,4aR,6aS,9aR,11R,13aR,13bS,15aS,15bR)-

Description:
1H-Cyclohepta[1,2-a:5,4-a']dinaphthalene-3,11-diol, also known by its CAS number 1449-06-5, is a complex polycyclic aromatic compound characterized by its unique fused ring structure. This compound features multiple fused naphthalene units, contributing to its stability and potential aromatic properties. The presence of hydroxyl (-OH) groups at specific positions indicates that it can engage in hydrogen bonding, which may influence its solubility and reactivity. The stereochemistry of the molecule, denoted by its specific chiral centers, suggests that it may exhibit distinct optical activity, which can be significant in biological systems or in applications such as pharmaceuticals. Additionally, the extensive methylation in its structure may enhance its hydrophobic characteristics, affecting its interaction with biological membranes and other organic compounds. Overall, this compound's intricate structure and functional groups make it a subject of interest in organic chemistry and materials science, particularly in studies related to its potential applications in drug development or as a precursor in synthetic chemistry.
Formula:C30H50O2
Synonyms:
  • 21-Episerratenediol(7CI)
  • C(14a)-Homo-27-norgammacer-14-ene-3,21-diol, (3b,21b)-
  • C(14a)-Homo-27-norgammacer-14-ene-3b,21b-diol (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-4,4,6a,10,10,13a,15b-heptamethyl-,[3S-(3a,4ab,6aa,9aa,11a,13ab,13ba,15ab,15ba)]-
  • 21-epi-Serratenediol
  • C(14a)-Homo-27-norgammacer-14-ene-3b,21b-diol
  • Serrat-14-en-3b,21b-diol
  • Serrat-14-ene-3b,21b-diol
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Purity (%)
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50
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90
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95
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100
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