Interesting facts
Interesting Facts about 2,2,2-Trifluoroethanamine
2,2,2-Trifluoroethanamine is a fascinating chemical compound that falls under the category of organofluorine compounds. Its unique structure and properties make it a noteworthy subject of study in various fields of chemistry. Here are some captivating insights about this compound:
- Fluorine Influence: The presence of three fluorine atoms significantly enhances the compound's stability and reactivity compared to other amines, which can lead to various applications in synthetic organic chemistry.
- Vue de la Structure: The trifluoro group attached to the ethylamine backbone contributes to its polar nature, making it an interesting candidate for studies involving intermolecular interactions.
- Biological Relevance: Fluorinated compounds, including 2,2,2-trifluoroethanamine, often show unique biological activities, drawing attention for their potential use in pharmaceuticals and agrochemicals.
- Applications: This compound can be employed in the synthesis of more complex molecules due to its ability to participate in various reactions, making it valuable in chemical research.
- Safety first: As with many fluorinated compounds, handling 2,2,2-trifluoroethanamine requires caution due to potential toxicity and environmental considerations.
In conclusion, 2,2,2-trifluoroethanamine stands out as a versatile compound with implications in both industrial and research settings. Its intriguing properties encourage further exploration and innovation in chemical synthesis, leading to potential breakthroughs in multiple scientific domains.
Synonyms
2,2,2-Trifluoroethylamine
753-90-2
Trifluoroethylamine
2,2,2-Trifluoroethanamine
Ethanamine, 2,2,2-trifluoro-
2,2,2-trifluoroethan-1-amine
2-Amino-1,1,1-trifluoroethane
ETHYLAMINE, 2,2,2-TRIFLUORO-
EINECS 212-041-3
BRN 1733204
DTXSID6061070
2,2,2-trifluoro-1-aminoethane
4-04-00-00442 (Beilstein Handbook Reference)
ethane, 1-amino-2,2,2-trifluoro-
MFCD00008132
2,2,2-trifluoroethyl amine
C2H4F3N
1-Amino-2,2,2-trifluoroethane
trifluoro ethylamine
trifluoroethyl amine
2,2,2-trifluorethylamine
2,2,2-trifluroethylamine
CF3CH2NH2
2.2.2-trifluoroethylamine
2,2,2,-trifluroethylamine
2,2,2-trifluoroethaneamine
2,2,2-Trifluoro-ethanamin
2, 2,2-trifluoroethylamine
2,2,2,-trifluoroethanamine
2,2,2,-trifluoroethylamine
2,2,2-trifluoro ethylamine
2,2,2-trifluoro-ethylamine
2,2,2-trifluoroethanaminium
2,2,2-trifluoroethane amine
(2,2,2-trifluoroethyl)amine
2,2,2-trifluoro ethyl amine
2,2,2-trifluoro-ethyl amine
2,2,2-trifluoro-ethyl-amine
2,2,2-Trifluoroethanamine #
44H2STW5P2
2,2,2-Trifluoro-1-ethanamine
CHEMBL1162282
DTXCID3047768
(2,2,2-trifluoro-ethyl)-amine
beta,beta,beta-Trifluoroethylamine
STR03274
FD2012
STL484274
2,2,2-Trifluoroethylamine, 99.5%
AKOS002528576
PB47403
.beta.,.beta.,.beta.-Trifluoroethylamine
BP-10752
DB-001190
NS00079909
T1169
EN300-34159
2,2,2-Trifluoroethylamine, >=98.0% (GC)
F2190-0538
212-041-3
Solubility of 2,2,2-trifluoroethanamine
2,2,2-trifluoroethanamine, known for its unique fluorinated structure, exhibits interesting solubility properties. Being a polar organic amine, its solubility can be influenced by various factors:
As a summary, it is crucial to remember that the solubility of 2,2,2-trifluoroethanamine is characterized primarily by its polarity and hydrogen bonding abilities, making it an interesting compound in various chemical applications.