Interesting facts
Interesting Facts about N-benzyl-N-ethyl-aniline
N-benzyl-N-ethyl-aniline, often referred to in scientific circles as a derivative of aniline, is a fascinating compound that has garnered attention for both its chemical structure and practical applications. Here are some compelling insights into this intriguing molecule:
- Structure and Composition: This compound features an aniline backbone, which is known for its significance in organic synthesis. The presence of both benzyl and ethyl substitutions contributes to its unique properties and reactivity.
- Applications: N-benzyl-N-ethyl-aniline is utilized in various fields, including:
- Organic Synthesis: It serves as a building block for synthesizing more complex molecules.
- Dyes and Pigments: The compound is used in the formulation of specific dyes, leveraging its ability to form colored products.
- Biological Relevance: Compounds in the aniline family have been studied for their biological activities. Some derivatives exhibit potential as:
- Pharmaceutical Agents: Certain analogs display promising characteristics as therapeutic agents.
- Antimicrobial Properties: There is ongoing research into their effectiveness against various pathogens.
- Chemical Stability: Due to the electron-donating characteristics of the ethyl and benzyl groups, N-benzyl-N-ethyl-aniline tends to exhibit remarkable stability in various chemical environments.
- Research and Development: The compound is often an area of interest in materials science and the development of novel chemical processes, further driving innovation in the synthesis of complex organic materials.
In summary, N-benzyl-N-ethyl-aniline is not just a simple compound; it bridges various fields of chemistry and possesses a versatile profile that makes it an exciting subject for research and application. As we continue to explore its properties and potential uses, this compound exemplifies the endless possibilities found within organic chemistry.
Synonyms
N-Benzyl-N-ethylaniline
92-59-1
Ethylbenzylaniline
N-ETHYL-N-BENZYLANILINE
N-Ethyl-N-phenylbenzylamine
Benzenemethanamine, N-ethyl-N-phenyl-
Benzylethylphenylamine
Phenylethylbenzylamine
Benzylamine, N-ethyl-N-phenyl-
N-Ethyl-n-phenyl benzylamine
Amine, benzyl ethyl phenyl
N-Ethyl-N-phenylbenzenemethanamine
NSC 1805
CCRIS 4649
HSDB 6120
EINECS 202-169-8
UN2274
N,N-Benzylethylaniline
AI3-10039
9E1613V4RO
NSC-1805
N-ethyl-N-benzyl-aniline
ETHYLBENZYLANILINE [MI]
DTXSID0025315
ETHYL-N-PHENYL BENZYLAMINE, N-
N-ETHYL-N-BENZYLANILINE [HSDB]
UNII-9E1613V4RO
Athylbenzylanilin
ethyl benzylaniline
NBenzylNethylaniline
NEthylNphenylbenzylamine
benzyl-ethyl-phenyl-amine
N-ethyl-N-benzyl aniline
Benzylamine, NethylNphenyl
N-Ethyl-N-benzylaniline [UN2274] [Poison]
N-Phenyl-N-ethylbenzylamine
BENZYLETHYL PHENYLAMINE
MLS001050175
NEthylNphenylbenzenemethanamine
SCHEMBL179996
DTXCID405315
N-benzyl-N-phenyl-N-ethylamine
CHEMBL1479610
N-Benzyl-N-ethylaniline, 99%
Benzenemethanamine, NethylNphenyl
NSC1805
AAA09259
Tox21_200375
MFCD00009037
NSC406962
AKOS008969357
Benzylamine, N-ethyl-N-phenyl-(8CI)
NSC-406962
UN 2274
CAS-92-59-1
NCGC00090897-01
NCGC00090897-02
NCGC00257929-01
BS-42307
SMR001216589
E0162
NS00008801
EN300-18363
N-Benzyl-N-ethylaniline, technical, >=97.0% (NT)
Q27272423
Z57770603
202-169-8
Solubility of N-benzyl-N-ethyl-aniline
N-benzyl-N-ethyl-aniline, a compound belonging to the class of anilines, exhibits interesting solubility characteristics that are influenced by its organic structure. Understanding the solubility of this compound can provide insights into its chemical behavior and potential applications.
General Solubility Characteristics
This compound is known to be:
Factors Influencing Solubility
The solubility of N-benzyl-N-ethyl-aniline can be attributed to several key factors:
As a rule of thumb, “like dissolves like,” which explains why N-benzyl-N-ethyl-aniline prefers non-polar environments. Understanding its solubility behavior is essential for applications in synthesis and extraction processes, where solvent choice can significantly affect the efficiency of reactions.