Interesting facts
Interesting Facts about 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene
This unique compound is a fascinating example of complex organic chemistry. With its intricate structure, 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene showcases the beauty of molecular engineering. Here are some intriguing aspects:
- Polycyclic Nature: The name indicates a highly branched structure composed of multiple linked rings, which is a characteristic feature of polycyclic compounds. This complexity can lead to unique chemical properties.
- Reactivity: The presence of double bonds in various configurations makes this compound particularly reactive. Such structural characteristics can influence reactions like electrophilic addition and oxidation.
- Applications: Compounds of this type are often studied for potential applications in organic electronics and materials science due to their ability to conduct electricity under certain conditions.
- Synthetic Challenges: Creating such a compound in the laboratory may pose numerous challenges, including manipulation of multiple reaction conditions, which can provide students and researchers with practical insights into synthetic organic chemistry.
- Biological Implications: While not all polycyclic compounds are biologically active, studying their structure can lend insight into drug design and discovery, potentially leading to innovations in pharmaceutical development.
- Interdisciplinary Interest: This compound bridges the gap between organic chemistry, material science, and pharmacology, making it a topic of interest for scientists from various fields.
In summary, the complexity and unique structure of 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene not only makes it a subject of vibrant academic interest but also underscores the intricate interplay between structure and function in the world of chemical compounds.
Synonyms
1155-38-0
7-Methylbenz(a)anthracene-5,6-oxide
Benz(a)anthracene, 5,6-dihydro-5,6-epoxy-7-methyl-
5,6-Epoxy-5,6-dihydro-7-methylbenz(a)anthracene
7-Methylbenz(a)anthracene 5,6-oxide
7-Methylbenz[a]anthracene 5,6-oxide
Benz[a]anthracene, 5,6-epoxy-5,6-dihydro-7-methyl-
BENZ(a)ANTHRACENE, 5,6-EPOXY-5,6-DIHYDRO-7-METHYL-
CCRIS 1118
7-Methylbenzanthracene 5,6-oxide
7-Methylbenz(a)anthracene 5,6 oxide
7-Methylbenz[a]anthracene 5,6-epoxide
1a,11b-Dihydro-11-methylbenz(3,4)anthra(1,2-b)oxirene
11-methyl-1a,11b-dihydrotetrapheno[5,6-b]oxirene
DTXSID30921739
MFBSRFKHKCKLIC-UHFFFAOYSA-N
Benz[3,4]anthra[1,2-b]oxirene, 1a,11b-dihydro-11-methyl-
11-Methyl-1a,11b-dihydrobenzo[3,4]anthra[1,2-b]oxirene #
19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene
Solubility of 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene
The solubility of complex organic compounds such as 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene is often influenced by several key factors:
In summary, predicting the solubility of 19-methyl-3-oxapentacyclo[9.8.0.02,4.05,10.013,18]nonadeca-1(19),5,7,9,11,13,15,17-octaene requires a thorough analysis of its molecular characteristics and the solvents in question.
As a general rule, nonpolar substances will exhibit better solubility in nonpolar solvents, and this compound exemplifies that principle within its complex framework.