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Fluoroethyl nitrosohydroxylamine methyl ether

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Identification
Molecular formula
C3H5F3N2O
CAS number
316-42-7
IUPAC name
N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide
State
State

At room temperature, Fluoroethyl nitrosohydroxylamine methyl ether is a liquid.

Melting point (Celsius)
-63.00
Melting point (Kelvin)
210.15
Boiling point (Celsius)
49.50
Boiling point (Kelvin)
322.65
General information
Molecular weight
153.08g/mol
Molar mass
153.0820g/mol
Density
1.2780g/cm3
Appearence

Fluoroethyl nitrosohydroxylamine methyl ether is a colorless liquid.

Comment on solubility

Solubility of N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide

N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide is a fascinating compound with unique solubility characteristics. The presence of the trifluoroethyl group significantly influences its solubility profile.

Key Points of Solubility

  • Polarity: Its structure introduces a polar trifluoromethyl group, enhancing solubility in polar solvents.
  • Common Solvents: This compound is generally soluble in polar organic solvents such as acetone, methanol, and dimethyl sulfoxide (DMSO).
  • Water Solubility: However, its solubility in water is relatively low due to the overall hydrophobic character contributed by the large fluorinated group.
  • Temperature Dependence: Like many organic compounds, the solubility may increase with temperature, making it easier to dissolve in warmer conditions.

To summarize, while N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide demonstrates good solubility in several polar organic solvents, its compatibility with water is limited. This unique behavior underscores the importance of considering both molecular structure and environmental conditions when assessing solubility.

Interesting facts

Interesting Facts about N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide

N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide is a fascinating compound with unique properties and applications in both organic chemistry and industry. Below are several aspects that elucidate its significance:

  • Unique Functional Groups: This compound showcases the presence of a nitrous amide group, which is notable for its ability to participate in a variety of chemical reactions. Its structure allows for specific interactions that can be exploited in synthetic pathways.
  • Fluorinated Compound: The trifluoroethyl group makes this compound particularly interesting due to the unique reactivity and stability that fluorinated compounds exhibit. Fluorine atoms can significantly alter a compound’s physical and chemical properties, such as lipophilicity and reactivity.
  • Potential Uses: Due to its distinct characteristics, N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide may find applications in materials science, pharmaceuticals, and agrochemicals. Research in these areas is ongoing, aiming to uncover more about its potential.
  • Environmental Considerations: As with other fluorinated compounds, there can be environmental concerns associated with their production and degradation. Scientists are increasingly interested in understanding these implications and finding sustainable alternatives.
  • Interdisciplinary Connections: The chemistry of this amide connects various fields, including medicinal chemistry, materials science, and environmental science, illustrating how a single compound can have wide-reaching impacts.

In conclusion, N-methyl-N-(2,2,2-trifluoroethyl)nitrous amide represents a compound rich in potential, offering both opportunities for innovative applications and challenges for environmental management. Its study is essential for advancing knowledge in chemical science.

Synonyms
Nitrosomethyl-2-trifluoroethylamine
819-35-2
ETHYLAMINE, N-METHYL-N-NITROSO-2,2,2-TRIFLUORO-
BRN 1764121
DTXSID00231453
DTXCID00153944