(4-nitrophenyl) N-ethylcarbamate

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Identification

Molecular formula
C9H10N2O4
CAS Number
59263-96-2
IUPAC Name
(4-nitrophenyl) N-ethylcarbamate
Molecular Weight
210.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3250g/cm3
Synonyms
4-Nitrophenyl ethylcarbamate
Interesting facts

Interesting Facts About (4-nitrophenyl) N-ethylcarbamate

(4-nitrophenyl) N-ethylcarbamate is a fascinating organic compound that falls under the category of carbamates. This class of compounds is known for its diverse applications, particularly in the fields of agriculture and pharmaceuticals. Here are some intriguing aspects of this particular compound:

  • Derived Features: The presence of a nitro group on the phenyl ring significantly influences the compound's properties. Nitro groups can enhance electron-withdrawing abilities, which can alter the reactivity and biological activity of the molecule.
  • Biological Activity: Carbamates are often evaluated for their potential as pesticides or herbicides. The interaction of (4-nitrophenyl) N-ethylcarbamate with various biological systems can yield important insights into its safety and efficacy in agricultural applications.
  • Mechanism of Action: Many carbamates function by inhibiting acetylcholinesterase, an enzyme critical for neurotransmission in both plants and animals. Studying (4-nitrophenyl) N-ethylcarbamate may reveal mechanisms that can be exploited for pest control strategies.
  • Research Applications: This compound can serve as a crucial intermediate in the synthesis of other chemicals, allowing chemists to explore novel organic transformations or develop new materials with tailored properties.

The study of (4-nitrophenyl) N-ethylcarbamate not only enhances our understanding of organic chemistry but also connects the dots to real-world applications that affect agriculture and pharmacology. As researchers continue to investigate its potential, one can only anticipate the exciting advancements that may arise from this compound!

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