Interesting facts
Interesting Facts about Ethyl 2-(3-nitroanilino)acetate
Ethyl 2-(3-nitroanilino)acetate is a fascinating compound that plays a significant role in various fields of chemistry and medicine. Here are some interesting insights about this compound:
- Functional Groups: This compound contains both an ester and an aniline group. The presence of these functional groups makes it a versatile molecule with different chemical reactivities and functions.
- Pharmaceutical Applications: Compounds with similar structures are often investigated for their potential as pharmaceuticals. They can act as intermediates in the synthesis of drugs or may possess biological activity themselves, making them of great interest in medicinal chemistry.
- Nitro Group: The 3-nitro substituent in the aniline moiety can significantly influence the electronic properties of the compound, often enhancing its reactivity and interaction with biological systems.
- Synthetic Utility: Ethyl 2-(3-nitroanilino)acetate can serve as a starting material in organic synthesis, particularly for the preparation of more complex organic molecules.
- Chemical Trends: Studying such compounds leads to a deeper understanding of structure-activity relationships (SAR) in chemistry, particularly in drug design and development.
As a chemist or a student, understanding the nuances of compounds like ethyl 2-(3-nitroanilino)acetate opens the door to numerous research opportunities and innovations in various scientific fields. It serves as a reminder of the complexity and beauty of chemical interactions.
Synonyms
GLYCINE, N-(m-NITROPHENYL)-, ETHYL ESTER
3589-58-0
ethyl 2-(3-nitroanilino)acetate
Ethyl N-(m-nitrophenyl)glycinate
ethyl {3-nitroanilino}acetate
BRN 2811849
Glycine, N-(3-nitrophenyl)-, ethyl ester
N-(m-Nitrophenyl)glycine ethyl ester
ethyl 2-((3-nitrophenyl)amino)acetate
ethyl 3-nitrophenylglycinate
SCHEMBL641425
DTXSID20189447
FOBXNGRQPJUTNJ-UHFFFAOYSA-N
phenylglycine, m-nitro- ethyl ester-
AKOS009135988
(3-nitro-phenylamino)-acetic acid ethyl ester
AG-205/05827037
Solubility of Ethyl 2-(3-nitroanilino)acetate
Ethyl 2-(3-nitroanilino)acetate, a compound known for its intriguing structure, exhibits varied solubility characteristics that are influenced by its functional groups. Understanding its solubility is key for its applications in chemical processes and reactions. Here are some important points to consider:
Due to the presence of nitro groups and the acetate moiety, this compound tends to be more soluble in polar solvents such as water and ethanol.
Conversely, ethyl 2-(3-nitroanilino)acetate is less soluble in non-polar solvents like hexane or benzene due to its polar functional groups, which do not interact favorably with non-polar environments.
Its solubility may also be affected by the pH of the solution, as the acidity can influence the ionization of functional groups, enhancing or reducing solubility depending on the conditions.
As with many organic compounds, increasing temperature typically increases solubility, so one might see improved interactions with solvents at elevated temperatures.
In summary, the solubility of ethyl 2-(3-nitroanilino)acetate is a multifaceted aspect influenced by solvent polarity, pH, and temperature. Understanding these factors allows chemists to optimize conditions for its use in various applications.