Interesting facts
Interesting Facts about (6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
(6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is a fascinating compound that occupies a unique position in the field of organic chemistry. Here are some intriguing insights about this complex structure:
- Structural Diversity: This compound exhibits a multi-ring structure that contributes to its rich chemical properties. The presence of both aromatic and saturated rings enhances its potential for interesting chemical reactions.
- Medicinal Relevance: Compounds with similar structures have been studied for their potential therapeutic benefits. Some dibenzoquinoline derivatives have shown promise in areas such as neurology and cancer research.
- Synthetic Pathways: The synthesis of dibenzoquinoline derivatives often involves complex reaction mechanisms including cyclization and functional group transformations, making this compound an exciting target for synthetic chemists.
- Pharmacophore Analysis: The specific arrangement of functional groups in (6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline may serve as a valuable pharmacophore for designing new drugs.
- Chirality: The (6aR) designation indicates that this compound is chiral, which is crucial in drug design as the different enantiomers can exhibit vastly different biological activities.
This compound stands as a testament to the intricate beauty of organic chemistry, showcasing how small changes in structure can lead to vastly different properties and potential applications. As researchers continue to explore its capabilities, the world of dibenzoquinoline derivatives remains an exciting frontier in chemical discovery.
Synonyms
Nuciferine
475-83-2
Nuciferin
l-Nuciferine
Sanjoinine E
(-)-nuciferine
(-)-Nucipherine
(R)-1,2-Dimethoxyaporphine
1,2-Dimethoxy-6abeta-aporphine
UNII-W26UEB90B7
W26UEB90B7
(6ar)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinoline
(R)-NUCIFERINE
D-(-)-NUCIFERINE
1-5, 6-Dimethoxyaporphine
4H-Dibenzo(de,g)quinoline, 5,6,6a,7-tetrahydro-1,2-dimethoxy-6-methyl-, (R)-
6a-beta-APORPHINE, 1,2-DIMETHOXY-
6a-.beta.-Aporphine, 1,2-dimethoxy-
1,2-DIMETHOXY-6A.BETA.-APORPHINE
4H-DIBENZO(DE,G)QUINOLINE, 5,6,6A,7-TETRAHYDRO-1,2-DIMETHOXY-6-METHYL-, (6AR)-
(6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo(de,g)quinoline
4H-Dibenzo(de,g)quinoline, 5,6,6a,7-tetrahydro-1,2-dimethoxy-6-methyl-, (R)-(9CI)
842-235-9
orjvqpihkoarkv-hnnxbmfysa-n
orjvqpihkoarkv-oahllokosa-n
(R)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
l-5,6-Dimethoxyaporphine
Nuciferine (Standard)
CHEMBL464529
Nuciferine - Bio-X trade mark
SCHEMBL20544868
HY-N0049R
HMS3887A19
HY-N0049
MSK40326
MFCD01664592
NSC785145
s3821
AKOS015903258
AC-7998
CCG-267422
CS-4270
FN65106
NSC-785145
1ST40326
BN300106
BS-42200
N1170
NS00067009
AG-690/36921306
Q7067904
Solubility of (6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline
The solubility of (6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is an intriguing topic due to its unique structural characteristics. This compound exhibits varying solubility patterns depending on the solvent used. Key factors influencing its solubility include:
In summary, while (6aR)-1,2-dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline is predominantly poorly soluble in polar solvents, it can dissolve well in nonpolar organic solvents due to its hydrophobic nature and the specific functional groups it contains.
Understanding the solubility characteristics can aid in the design and application of this compound in various chemical processes.