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Fenoxycarb

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Identification
Molecular formula
C17H19NO4
CAS number
72490-01-8
IUPAC name
(2-prop-2-ynoxyphenyl) N-methylcarbamate
State
State

At room temperature, Fenoxycarb is typically a solid. It may be presented as a fine powder depending on the chemical processing, handling, and storage conditions.

Melting point (Celsius)
46.50
Melting point (Kelvin)
319.65
Boiling point (Celsius)
367.00
Boiling point (Kelvin)
640.15
General information
Molecular weight
301.34g/mol
Molar mass
0.0000g/mol
Density
1.1578g/cm3
Appearence

Fenoxycarb appears as an off-white to light brown solid. It is usually encountered in a crystalline powder form and has no significant odor. This can vary slightly based on the level of purity and formulation conditions.

Comment on solubility

Solubility of (2-prop-2-ynoxyphenyl) N-methylcarbamate

The solubility of (2-prop-2-ynoxyphenyl) N-methylcarbamate can greatly affect its applications and behavior in various environments. Here are some key points about its solubility:

  • Solvent Dependence: This compound is likely to exhibit different solubility profiles in different solvents, including polar and non-polar mediums.
  • Temperature Effects: Solubility can be significantly influenced by temperature changes. Generally, an increase in temperature can enhance solubility for many organic compounds.
  • pH Influence: The pH of a solution can also play a critical role in solubility due to possible ionization, especially in cases of compounds containing nitrogen like N-methylcarbamate.
  • Hydrophilicity vs. Hydrophobicity: The balance of hydrophilic (water-attracting) and hydrophobic (water-repelling) components within the molecule affects its ability to dissolve in water versus organic solvents.
  • Practical Considerations: In practical applications, assessing solubility is crucial for determining appropriate dosage forms in pharmaceuticals or formulation in agrochemicals.

As a general principle, the more polar a molecule is, the more soluble it tends to be in polar solvents, while non-polar molecules prefer non-polar solvents. Therefore, understanding the specific interactions and chemical composition of (2-prop-2-ynoxyphenyl) N-methylcarbamate will be essential for optimizing its use in various chemical processes.

Interesting facts

Interesting Facts about (2-prop-2-ynoxyphenyl) N-methylcarbamate

(2-prop-2-ynoxyphenyl) N-methylcarbamate, often simply referred to as a carbamate derivative, is a fascinating compound that showcases unique chemical properties and applications.

Key Characteristics

  • Structural Diversity: This compound features a carbamate functional group, which is characterized by a carbonyl bonded to an amine and an alkoxy group. This structure contributes to its diverse reactivity.
  • Bioactivity: Carbamates are known for their biological activity. They often act as inhibitors of acetylcholinesterase, making them essential in the study of neurochemistry and potential pesticide applications.
  • Synthetic Utility: The presence of the prop-2-ynyl group in its structure offers opportunities for further chemical modification, enabling the synthesis of more complex derivatives that can be tailored for specific purposes.

Applications

The unique attributes of (2-prop-2-ynoxyphenyl) N-methylcarbamate extend to various fields:

  • Agricultural Science: Due to its potential inhibitory effects on cholinergic enzymes, it can be explored as a pesticide, providing an avenue for more environmentally friendly agricultural practices.
  • Pharmaceutical Research: The compound serves as a model for drug development, particularly in designing new medications that target neurodegenerative diseases.
  • Material Science: Research is ongoing into the use of carbamates in polymer chemistry, where they may enhance the properties of materials through cross-linking.

As stated by renowned chemist Linus Pauling, "The best way to have a good idea is to have lots of ideas." This resonates particularly with the study of such versatile compounds, which can pave the way for innovative advancements across multiple scientific disciplines.

Conclusion

The compound (2-prop-2-ynoxyphenyl) N-methylcarbamate epitomizes the dynamic nature of chemical research, where structural modifications can lead to breakthroughs in both science and industry. Continued exploration and understanding of its properties may unlock new potentials that benefit diverse fields.

Synonyms
Mcpop
Hercules 9699
o-(2-Propynyloxy)phenyl methylcarbamate
ENT 25,810
3279-46-7
Phenol, 2-(2-propynyloxy)-, methylcarbamate
H 9699
HE 9699
2-(2-Propynyloxy)phenol methylcarbamate
2-(2-Propynyloxy)phenyl methylcarbamate
CARBAMIC ACID, METHYL-, o-(2-PROPYNYLOXY)PHENYL ESTER
1XP20N155N
Caswell No. 714B
EPA Pesticide Chemical Code 314400
BRN 2053421
UNII-1XP20N155N
AI3-25810
SCHEMBL5566341
DTXSID7042223
LQLIPNNDDMXSGM-UHFFFAOYSA-N
ENT-25810
HE-9699
methylcarbamate2-(2-propynyloxy)-phenol
NS00123267
PROPYNYLOXY)PHENYL METHYLCARBAMATE, O-(2-
Q27253078