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methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate

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Identification
Molecular formula
C11H8Cl4NO4
CAS number
5278-35-9
IUPAC name
methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate
State
State

At room temperature, methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate is a solid compound. It is stable under normal conditions but should be stored in a cool, dry place to maintain its integrity. The compound does not readily evaporate or change under typical ambient conditions, maintaining its crystalline structure.

Melting point (Celsius)
95.00
Melting point (Kelvin)
368.15
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.15
General information
Molecular weight
365.99g/mol
Molar mass
365.9890g/mol
Density
1.7620g/cm3
Appearence

Methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate typically appears as a white to off-white crystalline powder. It has a distinct chemical odor that can be characteristic of benzoate compounds with chlorine substituents. The powder has a fine texture and is susceptible to changes in appearance at different environmental conditions.

Comment on solubility

Solubility Insights of Methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate

The solubility of methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate can be quite complex due to its intricate structure and the presence of various functional groups. Understanding its solubility characteristics is crucial for both practical applications and theoretical studies.

Factors Influencing Solubility

Several factors contribute to the solubility of this compound:

  • Polarity: The addition of chlorinated groups generally increases polarity, which can influence solubility in polar solvents.
  • Hydrogen Bonding: The methoxy and carbamoyl groups can participate in hydrogen bonding, potentially enhancing solubility in suitable solvents.
  • Solvent Choice: This compound may exhibit better solubility in organic solvents like acetone or ethyl acetate compared to water due to its hydrophobic characteristics.

Solubility Notes

While detailed experimental data on the solubility of this compound may be limited, general observations include:

  • Such chlorinated compounds typically show low solubility in water, owing to the hydrophobic aromatic ring.
  • In organic solvents, solubility can range from moderate to high, depending on the solvent's ability to disrupt intermolecular forces.

In summary, the solubility of methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate is influenced by its structural characteristics and the choice of solvent, making it essential to conduct specific solubility tests for practical applications.

Interesting facts

Interesting Facts about Methyl 2,3,5,6-Tetrachloro-4-[Methoxy(methyl)carbamoyl]benzoate

Methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate is a fascinating chemical compound that holds significance in various fields of chemistry and industry. Here are some intriguing aspects:

  • Insecticide Applications: This compound is often utilized as an insecticide, particularly effective in controlling a variety of pests. Its structure allows it to disrupt the biological functions of insects, making it a valuable tool in agriculture.
  • Complex Synthesis: The synthesis of this chemical can be quite intricate, involving multi-step reactions that require a deep understanding of organic chemistry principles. The presence of multiple chlorine substituents contributes to the compound's reactivity and stability.
  • Environmental Considerations: As with many chlorinated compounds, the environmental impact of methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate is a subject of study. Research is ongoing to assess its biodegradability and potential effects on non-target organisms in the ecosystem.
  • Commercial Use: Beyond its application in pest control, this compound also finds utility in the formulation of various products, enhancing efficacy and stability. It is an excellent example of how organic compounds can be tailored for specific industrial needs.
  • Biochemical Mechanism: Understanding how this compound interacts with biological systems is crucial. It primarily operates by affecting nervous system signals in pests, showcasing the compound's role as a neurotoxin. This mechanism is indicative of the broader category of organochlorine insecticides.

In summary, methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate represents the intersection of chemistry, agricultural science, and environmental studies. As it continues to be a topic of research, its diverse implications expand our understanding of compound interactions within ecosystems.

Synonyms
OCS-21,693
Methyl 2,3,5,6-tetrachloro-N-methoxy-N-methylterephthalamate
BRN 2162270
UNII-V87838EX37
OCS-21693
Methyl-2,3,5,6-tetrachloro-N-methoxy-N-methyl terephthalamate
OCS 21,693
V87838EX37
Terephthalamic acid, 2,3,5,6-tetrachloro-N-methoxy-N-methyl-, methyl ester
TEREPHTHALAMIC ACID, N-METHOXY-N-METHYL-2,3,5,6-TETRACHLORO-, METHYL ESTER
DTXSID7042144
Benzoic acid, 2,3,5,6-tetrachloro-4-((methoxymethylamino)carbonyl)-, methyl ester
Benzoic acid, 2,3,5,6-tetrachloro-4-[(methoxymethylamino)carbonyl]-, methyl ester
DTXCID5022144
Benzoic acid, 2,3,5,6-tetrachloro-4-((methoxymethylamino)carbonyl)-, methyl ester (9CI)
TMMT
14419-01-3
methyl 2,3,5,6-tetrachloro-4-[methoxy(methyl)carbamoyl]benzoate
N-Methoxy-N-methyl-2,3,5,6-tetrachloroterephthalamic acid methyl ester
SCHEMBL1873596
CWOBGOXHYZMVNY-UHFFFAOYSA-N
OCS 21693
NS00120869
Q27291663
Methyl 2,3,5,6-tetrachloro-4-([methoxy(methyl)amino]carbonyl)benzoate #