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Matolcarb

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Identification
Molecular formula
C12H16N2O5
CAS number
25313-89-5
IUPAC name
[3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate
State
State

At room temperature, Matolcarb exists in a solid crystalline state. It can be dissolved in certain organic solvents for further use in chemical reactions and manufacturing processes.

Melting point (Celsius)
53.00
Melting point (Kelvin)
326.15
Boiling point (Celsius)
332.30
Boiling point (Kelvin)
605.45
General information
Molecular weight
265.28g/mol
Molar mass
265.2750g/mol
Density
1.2480g/cm3
Appearence

Matolcarb typically appears as a colorless to yellowish crystalline solid. It may appear slightly different in industrial-grade forms due to impurities. It is usually handled in solid form to be utilized in manufacturing processes.

Comment on solubility

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

The solubility of the compound [3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate can be influenced by several factors, including its molecular structure and the presence of functional groups. Understanding its solubility is crucial for applications in pharmaceuticals and chemical industries.

Key Factors Affecting Solubility:

  • Hydrophilicity vs. Hydrophobicity: The methoxy and carbamate groups tend to enhance solubility in polar solvents due to their ability to form hydrogen bonds.
  • Temperature: As with many organic compounds, solubility generally increases with temperature, allowing for greater dissolution in solvents at elevated conditions.
  • pH Levels: The solubility can also vary based on the pH of the solution, particularly due to the ionization of the amino component in different environments.

It is often said that "like dissolves like." Therefore, polar solvents, such as water or alcohols, are likely to dissolve this compound more effectively compared to non-polar solvents due to its functional groups.

In summary, while comprehensive experimental data is required for precise solubility metrics, the presence of polar groups suggests that [3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate should exhibit moderate to good solubility in polar environments. This characteristic can be extremely beneficial for its applications in drug formulation and material science.

Interesting facts

Interesting Facts About [3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate

[3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate is a fascinating compound that showcases the intersection of organic chemistry and agricultural science. Here are some engaging aspects of this compound:

  • Pesticidal Properties: This compound is known for its role as a pesticide. Its molecular structure allows it to effectively target pests while minimizing harm to non-target organisms, making it an essential tool in sustainable agriculture.
  • Mechanism of Action: Its efficacy as a pesticide comes from its ability to inhibit certain enzymatic pathways in pests, disrupting their metabolism. This targeted action is crucial in modern pest management strategies!
  • Synthetic Pathways: The synthesis of this compound involves intricate multi-step organic chemical reactions. These pathways not only highlight the complexity of designing such molecules but also emphasize the ingenuity required in medicinal and agricultural chemistry.
  • Structure-Activity Relationship (SAR): The design encapsulates a prime example of SAR, where slight modifications in the chemical structure can lead to vastly different biological activities. Chemists study these relationships to optimize compounds for greater effectiveness and safety.
  • Research Implications: Continuing research into compounds like [3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate aids in the development of new solutions to combat resistant pest populations, enabling more effective and environmentally friendly pest control options.

As a compound that beautifully illustrates the importance of chemistry in addressing real-world agricultural challenges, [3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate stands as a testament to the advancements made in both chemical synthesis and ecological preservation.

Synonyms
19961-99-0
CARBANILIC ACID, m-HYDROXY-, 2-METHOXYETHYL ESTER, METHYLCARBAMATE
IOA0VT5U69
NSC 222639
BRN 2389620
m-Hydroxycarbanilic acid 2-methoxyethyl ester methylcarbamate
UNII-IOA0VT5U69
NSC-222639
2-Methoxyethyl m-hydroxycarbanilate, methylcarbamate
Carbanilic acid, m-hydroxy-, 2-methoxyethyl ester, methylcarbamate (ester)
DTXSID90173752
CARBAMIC ACID, METHYL-, ESTER WITH 2-METHOXYETHYL M-HYDROXYCARBANILATE
ETHANOL, 2-METHOXY-, M-HYDROXYCARBANILATE, METHYLCARBAMATE (ESTER)
DTXCID8096243
Carbanilic acid, m-hydroxy-, 2-methoxyethyl ester, methylcarbamate (ester) (8CI)
RefChem:123471
[3-(2-methoxyethoxycarbonylamino)phenyl] N-methylcarbamate
2-Methoxyethyl (3-((methylcarbamoyl)oxy)phenyl)carbamate
starbld0011241
2-Methoxyethyl m-hydroxycarbanilate methylcarbamate
orb1986295
NSC222639
AKOS040751020
Carbanilic acid, 2-methoxyethyl ester, methylcarbamate
Carbanilic acid, 2-methoxyethyl ester, methylcarbamate (ester)