Interesting facts
Interesting Facts about 9-methyl-9-azabicyclo[3.3.1]nonan-3-one
This fascinating compound, known as 9-methyl-9-azabicyclo[3.3.1]nonan-3-one, belongs to a unique class of bicyclic amines that are of great interest in organic chemistry. Here are some key points that make this compound stand out:
- Structural Uniqueness: The structure of 9-methyl-9-azabicyclo[3.3.1]nonan-3-one features a nitrogen atom embedded within a bicyclic framework, which significantly influences its chemical and physical properties.
- Functional Group Influence: The presence of the carbonyl group (ketone) combined with the bicyclic amine contributes to various reactivity patterns, making this compound a candidate for synthetic transformations in organic reactions.
- Pharmacological Potential: Compounds in this class may exhibit biological activities, and 9-methyl-9-azabicyclo[3.3.1]nonan-3-one could serve as a precursor for developing pharmacologically active agents, particularly in areas such as neurochemistry.
- Synthetic Applications: This compound can be utilized in the synthesis of more complex molecules, potentially serving as a building block in the development of new materials or pharmaceuticals.
- Research Interests: Ongoing studies explore the inherent properties of this compound, particularly its stereochemistry, which can impact interactions with biological targets.
To encapsulate the significance of 9-methyl-9-azabicyclo[3.3.1]nonan-3-one, one could say: "Such compounds, with their intricate molecular architectures, offer a window into the complexities of organic chemistry and the potential for innovation in drug development."
As our understanding of this compound deepens, it presents exciting opportunities for interdisciplinary research, intersecting organic synthesis, pharmacology, and material science.
Synonyms
9-Methyl-9-azabicyclo[3.3.1]nonan-3-one
Pseudopelletierine
552-70-5
Pseudopunicine
psi-Pelletierine
Pseudopelletrierin
Pseudopelletierin
Granatan-3-one
Granatonine
.psi.-Pelletierine
3-Granataninone, 9-methyl-
9-Methyl-3-granatanone
9-Azabicyclo[3.3.1]nonan-3-one, 9-methyl-
9-methyl-9-aza-bicyclo[3.3.1]nonan-3-one
9-Methyl-9-azabicyclo(3.3.1)nonan-3-one
NSC 116056
N-Methylgranatonine
Pseudopelletierin Hydrochloride
MFCD00078161
Y-Pelletierine
NSC-116056
Prestwick0_000625
Prestwick1_000625
Prestwick2_000625
Prestwick3_000625
9-Methyl-3-Granataninone
NCIOpen2_000165
BSPBio_000590
SCHEMBL551145
SPBio_002809
BPBio1_000650
CHEMBL2219893
RHWSKVCZXBAWLZ-UHFFFAOYSA-
DTXSID20870606
NSC116056
AKOS009156577
AC-2446
CS-W018069
HY-W017353
SB10982
NCGC00163612-01
NCGC00163612-02
CS-11004
DA-60634
SY001223
AB00514652
NS00043972
P2648
N-methyl-3-keto-9-azabicyclo[3.3.1]nonane
9-Methyl-9-azabicyclo[3.3.1]nonan-3-one #
9-Methyl-9-azabicyclo[3.3.1]nonan-3-one, 9CI
Q408775
SR-05000002308
SR-05000002308-2
BRD-A19053259-003-03-3
F8883-1415
InChI=1/C9H15NO/c1-10-7-3-2-4-8(10)6-9(11)5-7/h7-8H,2-6H2,1H3
Solubility of 9-methyl-9-azabicyclo[3.3.1]nonan-3-one
The solubility of 9-methyl-9-azabicyclo[3.3.1]nonan-3-one in various solvents presents interesting characteristics worth discussing. This compound, due to its unique bicyclic structure, engages with solvents in different ways:
In summary, the solubility of 9-methyl-9-azabicyclo[3.3.1]nonan-3-one varies with both the type of solvent and environmental conditions. Understanding these properties is crucial for effective applications in chemical processes.