Interesting facts
Exploring 2,2,3,3,4,4,4-Heptafluoro-N-phenyl-butanamide
2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide is a fascinating compound within the realm of fluorinated organic chemistries. Its unique structure incorporates both fluorine atoms and an aromatic phenyl group, making it a subject of great interest in various scientific fields. Let’s delve into some intriguing aspects of this compound:
- Fluorinated Properties: The introduction of multiple fluorine atoms significantly alters the chemical properties of the compound, enhancing its thermal stability and chemical inertness. This can lead to applications in high-performance materials.
- Relevance in Industry: Due to its unique characteristics, this compound may find uses in sectors such as pharmaceuticals, agrochemicals, and material science, contributing to innovations in drug formulation and pest control.
- Environmental Considerations: The use of fluorinated compounds often raises questions about environmental sustainability and toxicity. Research into this compound may provide insights into designing safer alternatives while retaining beneficial properties.
- Analytical Techniques: Scientists employ analytical techniques such as NMR spectroscopy and mass spectrometry to study the behavior and interactions of this compound, knowing how substituents like heptafluoro affect overall reactivity.
- Novel Applications: As research progresses, compounds like 2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide are being investigated for novel applications, including potential use in advanced polymers and specialty coatings.
In summary, 2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide exemplifies the complexity and multifaceted nature of fluorinated compounds. Its synthesis and characterization not only push the boundaries of organic chemistry but also pave the way for future advancements in material sciences and engineering.
Synonyms
Heptafluorobutyranilide
336-61-8
AI 3-18011
2,2,3,3,4,4,4-heptafluoro-N-phenylbutanamide
AI3-18011
Butyranilide, 2,2,3,3,4,4,4-heptafluoro-
FH26UK9AJK
NSC-404378
Butanamide, 2,2,3,3,4,4,4-heptafluoro-N-phenyl-
alpha,alpha,beta,beta,gamma,gamma,gamma-Heptafluorobutyranilide
BUTYRANILIDE, alpha,alpha,beta,beta,gamma,gamma,gamma-HEPTAFLUORO-
Butanamide, 2,2,3,3,4,4,4-heptafluoro-N-phenyl- (9CI)
NSC 404378
BRN 2751596
NSC404378
starbld0007507
UNII-FH26UK9AJK
WLN: FXFFXFFXFFVMR
4-12-00-00388 (Beilstein Handbook Reference)
Aniline, N-heptafluorobutyryl-
SCHEMBL8846991
DTXSID50187299
AKOS003625974
Butyranilide,2,3,3,4,4,4-heptafluoro-
DB-230507
NS00110522
Butanamide,2,3,3,4,4,4-heptafluoro-N-phenyl-
2,2,3,3,4,4,4-HEPTAFLUOROBUTYRANILIDE
Butyranilide,.alpha.,.beta.,.beta.,.gamma.,.gamma.,.gamma.-heptafluoro-
Butyranilide, .alpha.,.alpha.,.beta.,.beta.,.gamma.,.gamma.,.gamma.-heptafluoro-
Solubility of 2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide
The solubility of 2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide is a nuanced topic due to the compound's unique chemical structure. Composed of both hydrophobic and hydrophilic components, the solubility behavior can be described as follows:
In summary, the solubility of 2,2,3,3,4,4,4-heptafluoro-N-phenyl-butanamide is influenced by a balance between its fluorinated segments and the amide's capacity for hydrogen bonding. Therefore, it typically shows increased solubility in organic solvents while having limited solubility in aqueous environments. Further experimental studies are essential to precisely quantify its solubility characteristics under various conditions.