Interesting facts
Interesting Facts about 4-[3-(2-ethylhexylamino)-1-methyl-3-oxo-propoxy]-4-oxo-butanoic acid
This compound is a noteworthy member of the family of organic acids, specifically classified as an oxo-acid due to the presence of both carboxylic and ketone functional groups. Here are several key points about this fascinating compound:
- Biological Significance: The presence of amino groups within its structure suggests potential bioactivity, which can lead to interactions with various biological systems. Compounds like these are often evaluated for their pharmacological properties.
- Synthetic Utility: This compound can serve as an intermediate in the synthesis of more complex organic molecules. The functional groups present allow it to participate in various chemical reactions, such as esterifications or amide formations.
- Surfactant Potential: Given its amphiphilic structure combining hydrophobic and hydrophilic properties, this molecule may have applications in surfactants. Such compounds are essential in emulsification processes, detergents, and even pharmaceuticals.
- Structure-Activity Relationship (SAR): The unique configuration of the substituents on the aromatic ring opens discussions about how minor shifts can impact the molecule's activity in biological or catalytic processes, making it a relevant subject for research.
- Applications in Medicine: Due to its potential ability to interact with biological systems, researchers are interested in exploring this compound within the context of drug development, particularly in areas related to targeted delivery mechanisms.
Overall, 4-[3-(2-ethylhexylamino)-1-methyl-3-oxo-propoxy]-4-oxo-butanoic acid illustrates the richness of organic chemistry, where the interplay of various functional groups leads to myriad possibilities. As one could quote Albert Einstein, "Everything should be made as simple as possible, but not simpler." This embodies the spirit of studying complex compounds and discovering their simpler, underlying truths.
Synonyms
butoctamide semisuccinate
32838-28-1
Butoctamide hydrogen succinate
Listomin S
M-2H
Butoctamide hemisuccinate
BUTOCTAMIDE SUCCINATE
4-((4-((2-Ethylhexyl)amino)-4-oxobutan-2-yl)oxy)-4-oxobutanoic acid
Butoctamide semisuccinate [JAN]
N-2-Ethylhexyl-beta-oxybutyramide semisuccinate
DTXSID4057716
F58251NT6M
Butoctamide semisuccinate (JAN)
Listomin
UNII-F58251NT6M
Listomin S (TN)
N-(2-Ethylhexyl)-3-hydroxybutyramide hydrogen succinate
Succinic acid, monoester with N-(2-ethylhexyl)-3-hydroxybutyramide
CHEMBL3560122
DTXCID5031505
SCHEMBL22498725
CHEBI:31326
Tox21_113893
4-[3-(2-ethylhexylamino)-1-methyl-3-oxo-propoxy]-4-oxo-butanoic acid
AKOS026673906
Butanedioic acid, mono(3-((2-ethylhexyl)amino)-1-methyl-3-oxopropyl) ester
BUTOCTAMIDE SUCCINATE [WHO-DD]
NCGC00261973-01
BUTOCTAMIDE HYDROGEN SUCCINATE [MI]
CAS-32838-28-1
D01498
Q27114277
4-((4-((2-Ethylhexyl)amino)-4-oxobutan-2-yl)oxy)-4-oxobutanoicacid
BUTANEDIOIC ACID, 1-(3-((2-ETHYLHEXYL)AMINO)-1-METHYL-3-OXOPROPYL) ESTER
Solubility of 4-[3-(2-ethylhexylamino)-1-methyl-3-oxo-propoxy]-4-oxo-butanoic acid
The solubility of a compound is a critical factor that influences its behavior in various applications. For 4-[3-(2-ethylhexylamino)-1-methyl-3-oxo-propoxy]-4-oxo-butanoic acid (C16H29NO6), understanding its solubility characteristics can provide insights into its functionality.
Solubility Characteristics
In summary, the solubility of C16H29NO6 can be described as:
In practice, the solubility profile of this compound will greatly affect its reactivity and interaction in various chemical and biological systems. By understanding its solubility, practitioners can tailor its use to maximize effectiveness in desired applications.