Thiacloprid

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Identification

Molecular formula
C10H9ClN4S
CAS Number
111988-49-9
IUPAC Name
methyl N-[(2-aminoanilino)-sulfanyl-methylene]carbamate
Molecular Weight
252.74g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4600g/cm3
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.

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