Interesting facts
Interesting Facts about 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate; hydrochloride
This compound, commonly referred to in the scientific community, belongs to a class of organic compounds known for their diverse applications. Here are some fascinating points worth noting:
- Biological Activity: Compounds like this one often exhibit significant bioactivity, making them vital in pharmaceutical research. Their structure may allow them to interact with biological systems effectively.
- Synthetic Versatility: The synthesis of this compound involves various chemical reactions, showcasing the versatility of organic synthesis techniques. The presence of both an amine and a carboxylate functional group allows for modifications to create derivatives tailored for specific research needs.
- Applications in Research: This compound may be utilized in studies focusing on drug delivery systems and targeting mechanisms due to its structural properties. As noted by researchers, "the intricate design of certain organic compounds can open doors to new therapeutic strategies."
- Environmental Significance: Investigations into similar compounds have highlighted their roles in understanding environmental interactions, particularly concerning how chemical structures affect their behavior in biological systems.
- Educational Relevance: This compound serves as an excellent example in chemistry education for students learning about functional groups, aromatic compounds, and the role of substituents in altering chemical reactivity and properties.
In summary, 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate; hydrochloride is not just a compound but a fascinating subject of study that bridges various scientific disciplines, making it integral in advancing both theoretical and applied chemistry.
Synonyms
Naphthocaine hydrochloride
Naphthacaine hydrochloride
Naphthocaine HCl
UNII-96O81DVX5M
NSC 41652
96O81DVX5M
550-34-5
NSC-41652
4-Amino-1-naphthoic acid 2-(diethylamino)ethyl ester hydrochloride
DTXSID00203539
NSC41652
1-Naphthalenecarboxylic acid, 4-amino-, 2-(diethylamino)ethyl ester, monohydrochloride
1-NAPHTHOIC ACID, 4-AMINO-, 2-(DIETHYLAMINO)ETHYL ESTER, HYDROCHLORIDE
1-Naphthoic acid, 4-amino-, 2-(diethylamino)ethyl ester, monohydrochloride
DTXCID80126030
1-Naphthoic acid, 4-amino-, 2-(diethylamino)ethyl ester, monohydrochloride (8CI)
1-Naphthalenecarboxylic acid, 4-amino-, 2-(diethylamino)ethyl ester, monohydrochloride (9CI)
Q27271914
1-Naphthoic acid, 2-(diethylamino)ethyl ester, monohydrochloride
1-Naphthalenecarboxylic acid, 2-(diethylamino)ethyl ester, monohydrochloride
Solubility of 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate; hydrochloride
The solubility profile of 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate; hydrochloride is characterized by its intriguing interactions with solvents. Typically, this compound can be described as:
In aqueous solutions, the ionic character of the hydrochloride group contributes significantly to its solubility. This means that:
As a general observation, it is essential to consider that the pH of the solution can play a vital role in the solubility of this compound. Under acidic conditions, the solubility generally improves, whereas in basic conditions, precipitation may occur. As noted in solubility studies, "the balance between hydrophobic and hydrophilic interactions determines overall solubility behavior."
In summary, 2-(diethylamino)ethyl 4-aminonaphthalene-1-carboxylate; hydrochloride demonstrates significant solubility in water and polar organic solvents, making it useful for a variety of applications in both synthesis and biological systems.