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Oxamyl

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Identification
Molecular formula
C7H11NO3
CAS number
23135-22-0
IUPAC name
2-(1-phenylethylideneamino)oxyacetic acid
State
State
Oxamyl is generally encountered as a solid at room temperature, often appearing as colorless crystals. It is utilized as a pesticide.
Melting point (Celsius)
100.00
Melting point (Kelvin)
373.15
Boiling point (Celsius)
255.97
Boiling point (Kelvin)
529.12
General information
Molecular weight
219.24g/mol
Molar mass
219.2350g/mol
Density
1.2000g/cm3
Appearence

Oxamyl typically presents as a colorless crystalline solid.

Comment on solubility

Solubility of 2-(1-phenylethylideneamino)oxyacetic acid

When considering the solubility of 2-(1-phenylethylideneamino)oxyacetic acid, it is essential to take into account various factors that influence its behavior in different solvents. This compound's solubility can be characterized as:

  • Moderately soluble in water: Due to the presence of both acidic and basic functional groups, this compound can form hydrogen bonds with water, enhancing its solubility in polar solvents.
  • Soluble in organic solvents: 2-(1-phenylethylideneamino)oxyacetic acid demonstrates better solubility in organic solvents such as ethanol and acetone, which can interact favorably with its aromatic and aliphatic components.
  • pH-dependent solubility: The solubility of this compound can be significantly influenced by the pH of the solution. At lower pH levels, it may exist in a protonated form, while at higher pH levels, it can deprotonate, altering its solubility.

In summary, the solid-state and environmental conditions contribute to the solubility of 2-(1-phenylethylideneamino)oxyacetic acid, making it crucial for researchers to consider these factors when preparing solutions or conducting experiments.

Interesting facts

Interesting Facts about 2-(1-phenylethylideneamino)oxyacetic acid

2-(1-phenylethylideneamino)oxyacetic acid, often abbreviated as a complex organic compound, possesses a unique structure that makes it quite an intriguing subject of study in the realm of chemistry.

Chemical Significance

This compound showcases interesting characteristics influenced by the following components:

  • Amino Group: The presence of an amino group enhances its potential as a building block for larger molecules, often serving as a precursor in the synthesis of pharmaceuticals.
  • Phenylethylidene Moiety: This part of the molecule contributes to its aromatic properties, often influencing the compound's reactivity and interactions in biological systems.
  • Oxy Acid Functionality: The oxyacetic acid segment suggests potential acidity, enabling interesting behavior in various chemical reactions.

Biological Relevance

While specific biological activities of this compound may not be widely studied, many compounds with similar structures often exhibit:

  • Antioxidant Properties: Compounds with aromatic rings frequently display the ability to scavenge free radicals, which is crucial in mitigating oxidative stress.
  • Enzyme Inhibition: The amino and acid functionalities may interact with biological enzymes, influencing metabolic pathways.

Applications in Research

The synthetic pathways leading to 2-(1-phenylethylideneamino)oxyacetic acid are of particular interest in organic synthesis and medicinal chemistry:

  • This compound can serve as a template for designing novel drugs, particularly in the search for new treatments.
  • Researching similar compounds can lead to advances in understanding structure-activity relationships (SAR), aiding in drug development.

In summary, 2-(1-phenylethylideneamino)oxyacetic acid represents a fascinating intersection of organic chemistry and biological activity, serving as a potential precursor and model compound for further exploration in academic and pharmaceutical research.

Synonyms
1205-09-0
(Z)-2-(((1-phenylethylidene)amino)oxy)acetic acid
(Z)-2-(1-phenylethylideneaMinooxy)acetic acid
DTXSID601253652
AKOS017268894
AB89553