N,N-Dimethylthiocarbamoyl chloride

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Identification

Molecular formula
C3H6ClNS
CAS Number
1640-85-3
IUPAC Name
N,N-dimethylcarbamothioyl chloride
Molecular Weight
123.62g/mol
Melting Point
of -39°C.
Boiling Point
(Celsius)
Density
1.1920g/cm3
Synonyms
Dimethylthiocarbamoyl chloride
Interesting facts

N,N-Dimethylcarbamothioyl Chloride: A Unique Compound

N,N-Dimethylcarbamothioyl chloride is a fascinating compound that sits at the intersection of organic chemistry and industrial applications. Here are some interesting facts about this compound:

  • Functional Group Diversity: This compound features both a carbamothioyl group and a chloride, making it particularly significant in synthetic chemistry. Its structure allows for versatile reactivity, particularly in the formation of thioamide derivatives.
  • Role in Synthesis: It is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. The thioamide moiety can be crucial in the development of compounds with biological activity.
  • Reactivity: N,N-dimethylcarbamothioyl chloride exhibits reactivity typical of acyl chlorides, enabling it to participate in acylation reactions with nucleophiles. This property is advantageous in designing complex molecular architectures.
  • Historical Context: The study of compounds like N,N-dimethylcarbamothioyl chloride illustrates the broader evolution of chemical synthesis techniques over the decades, particularly during advancements in organic chemistry in the mid-20th century.
  • Safety Considerations: As a reagent, it is essential to handle N,N-dimethylcarbamothioyl chloride with caution due to its potential hazards. Proper lab safety protocols are necessary to mitigate risks associated with exposure.

In summary, N,N-dimethylcarbamothioyl chloride serves not only as an important reagent in organic synthesis but also embodies the intricate nature of chemical reactivity. Understanding compounds like this one enriches the field of chemistry and showcases the continual innovation in creating useful chemical entities.

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