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Fenoxycarb

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Identification
Molecular formula
C17H19NO4
CAS number
72490-01-8
IUPAC name
[3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate
State
State

At room temperature, Fenoxycarb is typically found in a solid state.

Melting point (Celsius)
59.00
Melting point (Kelvin)
332.15
Boiling point (Celsius)
392.90
Boiling point (Kelvin)
666.05
General information
Molecular weight
301.31g/mol
Molar mass
301.3120g/mol
Density
1.2200g/cm3
Appearence

Fenoxycarb is a white crystalline solid. It is often encountered in a powdered form and is relatively stable under normal conditions.

Comment on solubility

Solubility of [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate

The solubility of [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate in various solvents can provide crucial insight for its practical applications. This compound exhibits interesting solubility characteristics influenced by its structural components:

  • Polar Solvents: Generally, compounds containing amine groups like the N-methylcarbamate moiety often show increased solubility in polar solvents such as water or ethanol. However, the presence of the hydrophobic phenyl group may limit this solubility.
  • Non-polar Solvents: Due to the hydrophobic nature of the phenyl and the alkyne moiety, it may display better solubility in organic solvents such as hexane or chloroform.
  • pH Dependence: The solubility of this compound may also be pH-dependent, as the protonation state of the carbamate can vary in different pH environments, potentially altering its solubility profile.

In summary, the solubility of [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate can be affected by a variety of factors such as solvent polarity, temperature, and pH level. Understanding these factors is essential for optimizing the compound's use in various chemical contexts. As a rule of thumb, increasing polarity increases solubility in polar solvents, while non-polar characteristics favor solubility in organic solvents.

Interesting facts

Interesting Facts about [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate

[3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate is a fascinating compound that belongs to the broader class of carbamates, which are known for their diverse applications in both agriculture and pharmaceuticals. Here are some noteworthy aspects of this compound:

  • Unique Structure: The compound features a distinctive structure with a phenyl ring substituted with a prop-2-ynoxymethoxy group, providing potential reactivity and interaction with various biological systems.
  • Biological Activity: Carbamates, in general, have shown promise in the treatment of neurological disorders as acetylcholinesterase inhibitors. This suggests that [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate could have similar potential and is worth investigating for therapeutic applications.
  • Versatile Applications: Besides pharmaceutical uses, similar carbamate compounds are often used as herbicides and insecticides in agriculture, benefiting crop yield and pest control.
  • Research Potential: The unique functional groups in this compound can make it a subject of interest in medicinal chemistry, particularly in the design of new drugs targeting specific pathways.
  • Safety Considerations: While carbamates can be beneficial, they also require careful handling due to potential toxicity, underlining the importance of studying their effects in a controlled setting.

"The beauty of chemistry lies in its ability to create compounds that can significantly impact health and agriculture." This highlights the importance of compounds like [3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate in scientific exploration.

The exploration of this compound is not only vital for understanding its properties and applications but also for advancing our knowledge in the fields of chemistry and biological sciences. As researchers continue to study carbamates, we may uncover even more exciting potential that can benefit various industries.

Synonyms
18278-43-8
Hercules 9908
CARBAMIC ACID, METHYL-, m-((2-PROPYNYLOXY)METHOXY)PHENYL ESTER
m-((2-Propynyloxy)methoxy)phenyl methylcarbamate
DTXSID10171331
DTXCID7093822
[3-(prop-2-ynoxymethoxy)phenyl] N-methylcarbamate
3-((Prop-2-yn-1-yloxy)methoxy)phenyl methylcarbamate
starbld0048179
orb1697965
AKOS040751002
[3-(Prop-2-ynoxymethoxy)phenyl]n-methylcarbamate
Phenol, 3-[(2-propyn-1-yloxy)methoxy]-, 1-(N-methylcarbamate)