Interesting facts
Interesting Facts about (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-(4-chlorophenyl)prop-2-enoate; hydrochloride
As a member of the bicyclic compound family, (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-(4-chlorophenyl)prop-2-enoate; hydrochloride showcases the fascinating intersection of organic chemistry and pharmacology. Here’s why this compound is captivating:
- Unique Structure: The bicyclic structure of this compound makes it a subject of interest in the study of stereochemistry.
- Pharmacological Potential: Compounds like this one are often explored for their potential therapeutic uses, especially in neurology and psychiatry. They may exhibit properties beneficial for treating various cognitive disorders.
- Chirality: The presence of chiral centers in its structure allows for the potential of isomeric variations, which can significantly alter biological activity.
- Substituent Effects: The 4-chlorophenyl group introduces interesting electronic and steric effects, which can influence the compound's reactivity and interaction with biological targets.
In the realm of drug design, the exploration of such compounds often leads researchers to draw insights into:
- The interplay between chemical structure and biological activity.
- The development of targeted therapies that minimize side effects.
- How modifications in the molecular structure can enhance pharmacokinetic properties.
As one dives deeper into the world of chemical compounds, the study of derivatives like 8-methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(4-chlorophenyl)prop-2-enoate; hydrochloride can reveal profound implications in drug discovery, offering a glimpse into the complex mechanisms of life itself.
Synonyms
3-Tropanyl 2-(p-chlorophenyl)acrylate hydrochloride
SKF 21000
6746-91-4
SK&F 21000
3-Tropanyl 4'-chloroatropate hydrochloride
4'-Chloroatropic acid, 3-tropanyl ester, hydrochloride
1-alpha,5-alpha-Tropan-3-ol, p-chloroatropate (ester), hydrochloride
3-Tropanyl-2-(p-chlorophenyl)acrylate hydrochloride
Atropic acid, p-chloro-, 1-alpha-H,5-alpha-H-tropan-3-alpha-yl ester, hydrochloride
SK&F-21000
ATROPIC ACID, 4'-CHLORO-, 3-TROPANYL ESTER, HYDROCHLORIDE
3-tropanyl-2-(p-chlorophenyl)acrylate.HCl
Atropic acid, p-chloro-, 1-alpha-H,5-alpha-H-tropan-3-alpha-yl ester, hydrochloride (8CI)
(8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-(4-chlorophenyl)prop-2-enoate;hydrochloride
DTXSID50986729
Atropic acid, p-chloro-, tropyl ester, hydrochloride
8-Methyl-8-azabicyclo[3.2.1]octan-3-yl 2-(4-chlorophenyl)prop-2-enoate--hydrogen chloride (1/1)
Solubility of (8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 2-(4-chlorophenyl)prop-2-enoate; hydrochloride
The solubility of this compound is significantly influenced by its chemical structure, particularly the presence of the hydrochloride salt. In general, salts tend to have higher solubility in water compared to their parent bases. Key characteristics of this compound's solubility include:
In summary, while the compound can be expected to demonstrate good solubility owing to the hydrochloride form, the presence of hydrophobic substituents may create challenges in achieving maximum solubility in aqueous environments. It can be quoted that “the balance between hydrophilic and hydrophobic characteristics is crucial in determining overall solubility.”