Interesting facts
Interesting Facts about (3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene
This compound is part of a fascinating class of organic molecules known as polycyclic hydrocarbons. Here are some engaging points about this intriguing structure:
- Complex Structure: The nomenclature of this compound reveals its complexity. It has multiple chiral centers (indicated by the R and S designations), which suggests that its spatial arrangement can lead to a variety of stereoisomers.
- Potential Applications: Structures like this compound often exhibit interesting chemical properties that could be relevant in fields such as materials science, nanotechnology, or medicinal chemistry.
- Natural Products: Polycyclic compounds, especially those derived from cyclic structures, occur frequently in nature, often contributing to the coloration and functionality of various organic materials.
- Reactivity and Stability: Due to its saturated nature, this compound may offer insight into the reactivity patterns of similar saturated hydrocarbons, allowing for deeper understanding in organic reaction mechanisms.
- Chemical Derivatives: Exploring derivatives of this compound could lead to novel synthetic pathways and the creation of new materials with interesting physical or chemical properties.
Researchers focusing on polycyclic compounds often find them to possess unique properties, such as luminescence or advanced electrical characteristics. The exploration of such compounds can lead to significant breakthroughs in various scientific fields!
Synonyms
Hopane
A'-Neogammacerane
471-62-5
W2H93796GT
CHEBI:36482
DTXSID00904337
17.BETA.(H),21.BETA.(H)-HOPANE
(3R-(3.ALPHA.,3A.BETA.,5A.ALPHA.,5B.BETA.,7A.ALPHA.,11A.BETA.,11B.ALPHA.,13A.BETA.,13B.ALPHA.))-EICOSAHYDRO-5A,5B,8,8,11A,13B-HEXAMETHYL-3-(1-METHYLETHYL)-1H-CYCLOPENTA(A)CHRYSENE
1H-CYCLOPENTA(A)CHRYSENE, EICOSAHYDRO-5A,5B,8,8,11A,13B-HEXAMETHYL-3-(1-METHYLETHYL)-, (3R-(3.ALPHA.,3A.BETA.,5A.ALPHA.,5B.BETA.,7A.ALPHA.,11A.BETA.,11B.ALPHA.,13A.BETA.,13B.ALPHA.))-
DTXCID301333493
17BETA(H),21BETA(H)-HOPANE
(3R-(3ALPHA,3ABETA,5AALPHA,5BBETA,7AALPHA,11ABETA,11BALPHA,13ABETA,13BALPHA))-EICOSAHYDRO-5A,5B,8,8,11A,13B-HEXAMETHYL-3-(1-METHYLETHYL)-1H-CYCLOPENTA(A)CHRYSENE
1H-CYCLOPENTA(A)CHRYSENE, EICOSAHYDRO-5A,5B,8,8,11A,13B-HEXAMETHYL-3-(1-METHYLETHYL)-, (3R-(3ALPHA,3ABETA,5AALPHA,5BBETA,7AALPHA,11ABETA,11BALPHA,13ABETA,13BALPHA))-
zrlnbwwglopjic-uhfffaoysa-n
(3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-5a,5b,8,8,11a,13b-hexamethyl-3-propan-2-yl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene
UNII-W2H93796GT
US11660306, Example hopane
BDBM604159
17 beta (H),21 beta (H)-Hopane solution
Q5898987
Solubility of (3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene
The solubility of the compound (3R,3aS,5aR,5bR,7aS,11aS,11bR,13aR,13bS)-3-isopropyl-5a,5b,8,8,11a,13b-hexamethyl-1,2,3,3a,4,5,6,7,7a,9,10,11,11b,12,13,13a-hexadecahydrocyclopenta[a]chrysene is influenced by several factors given its complex structure. This compound is expected to exhibit low solubility in polar solvents due to its large hydrophobic regions. However, it may show greater solubility in non-polar organic solvents.
Key Points on Solubility:
In conclusion, understanding the solubility of this complex compound requires a careful consideration of its chemical structure and the polarity of solvents. As such, it plays a crucial role in its potential applications, especially in organic synthesis and material science.