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2-fluoroethyl N-(1-naphthyl)carbamate

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Identification
Molecular formula
C13H12FNO2
CAS number
2252-49-3
IUPAC name
2-fluoroethyl N-(1-naphthyl)carbamate
State
State

2-Fluoroethyl N-(1-naphthyl)carbamate is generally in a solid state at room temperature.

Melting point (Celsius)
83.00
Melting point (Kelvin)
356.15
Boiling point (Celsius)
365.50
Boiling point (Kelvin)
638.65
General information
Molecular weight
233.24g/mol
Molar mass
233.2430g/mol
Density
1.2110g/cm3
Appearence

2-Fluoroethyl N-(1-naphthyl)carbamate typically appears as a solid at room temperature. The color can range from white to off-white, depending on the purity and form of the sample. It is usually crystalline in nature.

Comment on solubility

Solubility of 2-fluoroethyl N-(1-naphthyl)carbamate

2-fluoroethyl N-(1-naphthyl)carbamate, a compound characterized by its unique structure, exhibits notable solubility properties. Understanding its solubility can provide insights into its practical applications and behavior in different environments.

Key Aspects of Solubility:

  • Polar vs. Non-Polar: The presence of both a polar carbamate group and the non-polar naphthyl moiety influences its solubility in solvents. It is likely to have varying solubility in polar and non-polar solvents.
  • Solvent Compatibility: It may dissolve more readily in organic solvents like ethanol and acetone than in water, due to the hydrophobic nature of the naphthyl group.
  • Temperature Effects: Temperature can play a crucial role in its solubility; an increase in temperature typically increases the solubility of organic compounds.
  • Concentration Considerations: At higher concentrations, solubility limits may be reached, leading to potential precipitation or phase separation in solutions.

In summary, while 2-fluoroethyl N-(1-naphthyl)carbamate shows versatility in solubility, its behavior in various solvents should be studied carefully to optimize its use in relevant applications. Its solubility characteristics are essential for ensuring effective formulation and reactivity in chemical processes.

Interesting facts

Interesting Facts about 2-Fluoroethyl N-(1-naphthyl)carbamate

2-Fluoroethyl N-(1-naphthyl)carbamate is a fascinating compound that falls within the category of carbamates, known for their diverse applications in various fields. Here are some intriguing aspects of this compound:

  • Carbamate Classification: As a member of the carbamate family, it features a carbonyl group bonded to a nitrogen atom, which is also connected to a naphthyl group. This unique structure allows for a variety of chemical reactivities.
  • Fluorine's Role: The presence of the fluoroethyl group marks it as a compound of interest in medicinal chemistry. Fluorine is known to enhance the biological activity and membrane permeability of compounds, making it a potent element in the development of pharmaceuticals.
  • Potential Applications: This compound could be explored for its potential as an insecticide or herbicide, similar to other carbamate-based pesticides. Its structure may confer specific pest-targeting capabilities, leading to effective crop protection.
  • Research Significance: Studies on carbamates have revealed their importance in neurological research, as certain carbamate compounds can act as inhibitors of acetylcholinesterase, which plays a critical role in neurotransmission.
  • Environmental Considerations: Understanding the behavior and breakdown of such compounds in the environment is crucial. Investigating their stability, degradation pathways, and potential toxicity helps in assessing ecological risk.

Researchers are continually discovering new applications for compounds like 2-fluoroethyl N-(1-naphthyl)carbamate. As noted in various studies, "The unique properties and performance of carbamates offer a promising avenue for the development of advanced materials and pharmaceuticals." This compound exemplifies the intersection of chemistry and real-world applications, showing just how intricate and impactful chemical research can be.

Synonyms
343-47-5
1-Naphthalenecarbamic acid, 2-fluoroethyl ester
CARBAMIC ACID, N-(alpha-NAPHTHYL)-, 2-FLUOROETHYL ESTER
2-fluoroethyl N-naphthalen-1-ylcarbamate
NSC 106895
BRN 3310935
beta-Fluoroethyl, N-(alpha-naphthyl)carbamate
(1-Naphthyl)carbamic acid 2-(fluoroethyl)ester
1-Naphthylcarbamic acid, ester with 2-fluoroethanol
Carbamic acid, (1-naphthyl)-, 2-(fluoroethyl)ester
WLN: L66J BMVO2F
DTXSID00187860
Carbamic acid, 2-fluoroethyl ester
NSC106895
NSC-106895
.beta.-fluoroethyl, N-(.alpha.-naphthyl)carbamate