Interesting facts
Exploring Azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone
Azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone is a fascinating compound that showcases the intricate world of synthetic organic chemistry. Here are some intriguing highlights about this compound:
- Hybrid Structure: This compound combines the azocane ring, which is a saturated nitrogen-containing heterocycle, with a trimethoxyphenyl group. This unique structure makes it a target for various studies.
- Potential Applications: Given its energetic framework, this compound is of interest in the development of novel materials, especially in fields like pharmaceuticals and organic electronics.
- Synthetic Routes: The synthesis of azocan derivatives often involves various reaction techniques, including nucleophilic substitution and condensation reactions. This showcases the versatility of organic synthesis methodologies.
- Biological Significance: Compounds with similar structures have been researched for their biological activities, including antimicrobial and anticancer properties. This makes azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone a candidate for future pharmaceutical research.
In the words of renowned chemist Linus Pauling, “Science is a search for the simple laws which govern the complex phenomena of nature.” Azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone exemplifies this principle, representing how complex organic compounds can lead to significant discoveries in science and medicine.
As we continue to explore compounds like this, we uncover not just their individual properties but also how they contribute to the broader landscape of organic chemistry and material science.
Synonyms
Trocimine
Origen
Origon
Trocimine [INN]
Trocimina
Trociminum
Trociminum [INN-Latin]
Trocimina [INN-Spanish]
Octahydro-1-(3,4,5-trimethoxybenzoyl)azocine
N 1157
N-(3,4,5-Trimethoxybenzoyl)azacyclooctane
1-(3,4,5-Trimethoxybenzoyl)octahydroazocine
UNII-8EE22OKO88
N-(3,4,5-Trimethoxybenzoyl)heptamethylenimine
N-(3,4,5-Trimethoxybenzoyl)heptamethyleneimine
NSC 233082
NSC-233082
BRN 1394755
8EE22OKO88
DTXSID1046475
AZOCINE, OCTAHYDRO-1-(3,4,5-TRIMETHOXYBENZOYL)-
N-3,4,5-trimethoxybenzoyl-heptamethylene imine
DTXCID9026475
5-20-04-00162 (Beilstein Handbook Reference)
Trociminum (INN-Latin)
Trocimina (INN-Spanish)
N-(3,4,5-Trimethoxybenzoyl)heptamethylenimin
WZSDNEJJUSYNSG-UHFFFAOYSA-N
14368-24-2
azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone
N-1157
NCGC00164606-01
CAS-14368-24-2
SCHEMBL9534
CHEMBL1974057
Azocine,4,5-trimethoxybenzoyl)-
Tox21_112228
NSC233082
STK491079
AKOS003376686
N-(3,4,5-trimethoxybenzoyl)azocidine
Tox21_112228_1
WLN: T8NTJ AVR CO1 DO1 EO1
N-(3,5-Trimethoxybenzoyl)azacyclooctane
NCGC00164606-02
N-3,5-Trimethoxybenzoylheptamethylenimine
N-(3,5-Trimethoxybenzoyl)heptamethylenimine
Octahydro-1-(3,5-trimethoxybenzoyl)azocine
N-(3,5-Trimethoxybenzoyl)heptamethyleneimine
NS00126530
ST50884978
azocan-1-yl(3,4,5-trimethoxyphenyl)methanone
azaperhydroocinyl 3,4,5-trimethoxyphenyl ketone
SR-01000883954
1-AZOCANYL(3,4,5-TRIMETHOXYPHENYL)METHANONE
SR-01000883954-1
Q27270254
Solubility of Azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone
The solubility of azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone can be characterized by several important factors:
In summary, understanding the solubility of azocan-1-yl-(3,4,5-trimethoxyphenyl)methanone is crucial for applications in synthesis and analysis. Proper selection of solvent, consideration of temperature, and monitoring of pH can significantly enhance its usability in various chemical processes.