Interesting facts
N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide
N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is a compound that showcases the fascinating interplay between organic chemistry and material science. Here are some intriguing facts that highlight its significance:
- Fluorine Influence: The presence of fluorine atoms in this compound significantly alters its chemical properties. Fluorine is known for its electronegativity, which can influence the reactivity and stability of organic molecules.
- Potential Applications: Compounds like N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide could have applications in various fields, such as:
- Medicinal chemistry
- Polymer science
- Material fabrication
- Synthesis and Reactions: Its synthesis involves amino chemistry, whereby functional groups are introduced to create complex molecules, making it an interesting compound for students studying organic synthesis.
- Structure and Function Relationship: Understanding the relationship between the compound's structure and its anticipated properties can help researchers develop new materials with tailored functions for specific applications.
As stated by a renowned chemist, “The beauty of chemistry lies in its ability to create and manipulate molecules in innovative ways.” This compound exemplifies how careful design can lead to functional compounds that play critical roles in scientific advancements.
Overall, N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is not merely a chemical entity but a showcase of the vast possibilities within the realm of chemistry.
Synonyms
363-17-7
N-(2-Fluorenyl)-2,2,2-trifluoroacetamide
N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide
2-Trifluoroacetylaminofluorene
N-Fluoren-2-yl-2,2,2-trifluoroacetamide
2,2,2-Trifluoro-N-(fluoren-2-yl)acetamide
ACETAMIDE, N-FLUOREN-2-YL-2,2,2-TRIFLUORO-
N-9H-fluoren-2-yl-2,2,2-trifluoroacetamide
Acetamide, N-9H-fluoren-2-yl-2,2,2-trifluoro-
2-(2,2,2-Trifluoroacetamido)fluorene
DTXSID3020629
454X3J3CX8
NSC-12283
2-((Trifluoroacetyl)amino)fluorene
2-[(Trifluoroacetyl)amino]fluorene
NSC 12283
BRN 2814131
2-Aminofluorene, TFA
CHEMBL82129
DTXCID70629
UNII-454X3J3CX8
WLN: L B656 HHJ EMVXFFF
NSC12283
Tox21_301891
AKOS009038699
N-(2-Fluorenyl)-2,2-trifluoroacetamide
NCGC00255119-01
CAS-363-17-7
2,2-Trifluoro-N-(fluoren-2-yl)acetamide
DS-006332
NS00126685
Fluorenyl)-2,2,2-trifluoroacetamide, N-(2-
Acetamide,n-9h-fluoren-2-yl-2,2,2-trifluoro-
N-(9H-Fluoren-2-yl)-2,2,2-trifluoroacetamide #
Q63088208
632-237-6
Solubility of N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide
N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is a compound that showcases unique solubility characteristics due to its molecular structure and the presence of multiple functional groups. Understanding the solubility of this compound is crucial for its applications in various chemical processes.
In summary, solubility of N-(9H-fluoren-2-yl)-2,2,2-trifluoro-acetamide is influenced by its polarity, functional groups, and the nature of the solvent used. Understanding these factors is key for optimizing its use in different chemical environments.