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Thiacloprid

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Identification
Molecular formula
C10H9ClN4S
CAS number
111988-49-9
IUPAC name
methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate
State
State

At room temperature, Thiacloprid exists as a solid, typically in a powdered form.

Melting point (Celsius)
136.50
Melting point (Kelvin)
409.65
Boiling point (Celsius)
407.00
Boiling point (Kelvin)
680.15
General information
Molecular weight
252.74g/mol
Molar mass
252.7400g/mol
Density
1.4600g/cm3
Appearence

Thiacloprid is a white to beige powder that is crystalline in nature. It is generally odorless.

Comment on solubility

Solubility of Methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate

Methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate is an intriguing compound whose solubility can be influenced by several factors. Understanding the solubility characteristics can provide insight into its potential applications and behavior in various environments.

When evaluating the solubility of this compound, consider the following aspects:

  • Polarity: The presence of both carbamate functional groups and amino groups can affect the polarity of the compound, which in turn impacts its solubility in different solvents. Compounds with higher polarity tend to be more soluble in polar solvents like water.
  • Hydrogen Bonding: The ability to form multiple hydrogen bonds with solvent molecules may enhance solubility. The amino group may engage in hydrogen bonding, facilitating interactions with water molecules.
  • Solvent Choice: Solubility may vary significantly between solvents. For instance, this compound may exhibit greater solubility in alcohols or slightly polar organic solvents compared to nonpolar solvents.
  • Temperature Effects: The solubility of many compounds can be temperature-dependent. Typically, increased temperature can lead to higher solubility, but this is not a universal rule.

In summary, the solubility profile of methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate is complex and may vary widely based on the aforementioned factors. Experimentally determining its solubility in different solvents will be crucial for its practical applications.

Interesting facts

Interesting Facts about Methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate

Methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate is a fascinating compound that showcases the versatility of organic chemistry, particularly in the realm of medicinal research. Here are some intriguing insights:

  • Amino Group Interactions: The presence of the amino group in this compound allows it to engage in hydrogen bonding, which can enhance its biological activity and interaction with targeted biomolecules.
  • Sulfanyl Moiety: The sulfanyl group endows this compound with unique chemical properties. It has been shown to participate in nucleophilic attack, making it useful in various chemical reactions.
  • Potential Applications: Compounds similar to methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate are often explored for their potential as pharmaceuticals. Researchers are continually investigating their roles as enzyme inhibitors or as therapeutic agents against various diseases.
  • Importance in Agricultural Chemistry: Due to its structural characteristics, this compound may also have applications in agrochemicals, enhancing pest resistance in crops.
  • Research Interest: As a subject of ongoing studies, it exemplifies the role of structural modifications in altering the function and efficacy of biologically active compounds. Scientists are keen to understand how small changes in the molecular structure can impact the compound's properties.

In summary, methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate richly illustrates the dynamic interplay between structure and function in chemistry. As scientists continue to explore its properties, this compound stands as a testament to the innovative possibilities within the field of chemical research.