Interesting facts
Interesting Facts about 4-Chloro-N-(2-hydroxyethyl)-N-[(3-methylnorbornan-2-yl)methyl]benzamide
This compound is a fascinating member of the amide functional group that has garnered attention due to its diverse applications in various fields such as pharmaceuticals and material science. Let’s delve into some intriguing aspects of this interesting molecule:
- Structural Diversity: The presence of both a chloro group and a hydroxyalkyl substituent makes this compound structurally unique, allowing it to interact with various biological systems effectively.
- Potential Medical Applications: Compounds like this one are often evaluated for their potential as drug candidates. Their ability to modify biological pathways may be exploited in treating conditions such as cancer or neurodegenerative diseases.
- Chiral Centers: This compound features chiral centers, which add complexity to its synthesis and potential interactions. Chirality plays a crucial role in pharmacodynamics, as different enantiomers can exhibit vastly different biological activities.
- Interaction with Receptors: The hydroxyethyl group may enhance the solubility and biological availability of the compound, improving its interaction with specific receptors in the body.
- Polymer Science: Due to its functional groups, it could serve as a precursor for polymers with tailored properties, demonstrating the versatility of amides in materials development.
In summary, 4-chloro-N-(2-hydroxyethyl)-N-[(3-methylnorbornan-2-yl)methyl]benzamide exemplifies the intricate relationship between structure and functionality in chemical compounds. As noted, “The chemist’s language is structure,” and this compound speaks volumes about the elegance of organic chemistry!
Synonyms
Clocanfamide
Chlorocamphamide
Clocanfamida
Clomiren
Clocanfamide [INN]
Clocanfamidum
Clocanfamidum [INN-Latin]
Clocanfamida [INN-Spanish]
UNII-21Q62BRI9U
BRN 2757291
21Q62BRI9U
p-Chloro-N-(2-hydroxyethyl)-N-((3-methyl-2-norbornyl)methyl)benzamide
Clocanfamidum (INN-Latin)
Clocanfamida (INN-Spanish)
Benzamide, 4-chloro-N-(2-hydroxyethyl)-N-((3-methylbicyclo(2.2.1)hept-2-yl)methyl)-
BENZAMIDE, p-CHLORO-N-(2-HYDROXYETHYL)-N-((3-METHYL-2-NORBORNYL)METHYL)-
Benzamide, 4-chloro-N-(2-hydroxyethyl)-N-((3-methylbicyclo(2.2.1)hept-2-yl)methyl)-(9CI)
18966-32-0
Clorocanfamide
4-chloro-N-(2-hydroxyethyl)-N-[(3-methyl-2-bicyclo[2.2.1]heptanyl)methyl]benzamide
SCHEMBL2111073
CHEMBL2104134
DTXSID60864867
p-Chlor-N-(2-hydroxyethyl)-N-(3-methylnorborn-2-ylmethyl)benzamide
NS00123186
Q27253568
Solubility of 4-chloro-N-(2-hydroxyethyl)-N-[(3-methylnorbornan-2-yl)methyl]benzamide
The solubility of 4-chloro-N-(2-hydroxyethyl)-N-[(3-methylnorbornan-2-yl)methyl]benzamide can be quite complex due to its intricate molecular structure. Here are several factors that influence its solubility:
As a general observation, compounds of this nature often exhibit limited solubility in water while being more soluble in organic solvents due to the conflicting impacts of their polar and nonpolar regions. Hence, careful consideration should be given to the medium used for dissolution.