Aldicarb

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Identification

Molecular formula
C7H14N2O2S2
CAS Number
116-06-3
IUPAC Name
[(2,4-dimethyl-1,3-dithiolan-2-yl)methyleneamino] N-methylcarbamate
Molecular Weight
190.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1950g/cm3
Synonyms
[(2, 4-dimethyl-1, 3-dithiolan-2-yl)methylideneamino] N-methylcarbamate
Interesting facts

Interesting Facts about [(2,4-dimethyl-1,3-dithiolan-2-yl)methyleneamino] N-methylcarbamate

The compound [(2,4-dimethyl-1,3-dithiolan-2-yl)methyleneamino] N-methylcarbamate is a fascinating example of a carbamate derivative with unique structural characteristics and potential applications in various fields.

  • Biological Significance: This compound exhibits potential biological activity, particularly in the field of agrochemicals. Its structure may allow it to act as an insecticide or herbicide, making it valuable for agricultural practices.
  • Synthetic Pathways: The synthesis of this compound involves intricate organic chemistry techniques, often requiring precision in controlling reaction conditions and purity of reactants. Its preparation highlights the challenges and creativity inherent in chemical synthesis.
  • Functional Group Features: The dithiolan ring is not just a structural feature; it introduces interesting electronic properties to the compound. This might influence its reactivity and interactions with biological targets.
  • Environmental Applications: Compounds like this are being explored for environmentally friendly pest control. Understanding their mechanisms can lead to sustainable solutions in agricultural chemistry.

As a chemical scientist or student, one might reflect on the importance of the carbamate functional group. As noted by many in the field, "the derivatives of carbamic acid are crucial in developing bioactive compounds." This highlights the relevance of compounds like [(2,4-dimethyl-1,3-dithiolan-2-yl)methyleneamino] N-methylcarbamate in the ongoing quest for safer and more effective agrochemicals.

In summary, studying this compound not only deepens our understanding of organic chemistry and synthetic methods but also reinforces the links between chemistry, biology, and environmental science.

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