Pendimethalin

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Identification

Molecular formula
C13H19ClN2O4
CAS Number
40487-42-1
IUPAC Name
N-(2-chloroethyl)-2,4-dinitro-aniline
Molecular Weight
281.70g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2346g/cm3
Synonyms
N-(2-Chloroethyl)-2, 4-dinitroaniline
Interesting facts

Interesting Facts About N-(2-Chloroethyl)-2,4-Dinitro-Aniline

N-(2-Chloroethyl)-2,4-dinitro-aniline is a fascinating organic compound with diverse applications and implications in both chemistry and industry. Here are some noteworthy elements about this compound:

  • Pharmaceutical Significance: The compound is often explored for its potential therapeutic properties, offering insights into how modifications in chemical structures can yield drugs with enhanced efficacy and reduced side effects.
  • Disruptor of Biological Systems: This compound contains a chloroethyl group, known to be a reactive moiety that can interact with various biomolecules. Such interactions can lead to important studies in drug resistance and toxicology.
  • Environmental Impact: Compounds like N-(2-chloroethyl)-2,4-dinitro-aniline are subjected to scrutiny for their environmental persistence and potential hazardous effects. Understanding their breakdown and interaction with ecosystems is imperative.
  • Historical Context: The synthesis and study of dinitroaniline derivatives date back to the early 20th century, during which time the field of synthetic organic chemistry was blossoming, notably influencing agriculture and chemical warfare.

In many cases, the presence of nitro groups within the structure can impart strong electrophilic characteristics, making these compounds useful in various chemical reactions, including the formation of advanced materials. As researchers continue to explore the multifaceted nature of such chemical entities, N-(2-chloroethyl)-2,4-dinitro-aniline stands out as a compound rich with potential and pitfalls alike.

Potential Future Research Areas

Future studies may focus on:

  • Developing safer alternatives to compounds derived from chloroethyl groups.
  • Investigating the compound's role as a metabolic substrate in various biological pathways.
  • Exploring its utility in the synthesis of novel materials or dyes.

As science progresses, the multifaceted roles and behaviors of N-(2-chloroethyl)-2,4-dinitro-aniline will likely continue to be a subject of keen interest!

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