Cyclophosphamide

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Identification

Molecular formula
C8H10Cl2O4
CAS Number
111-48-8
IUPAC Name
bis(2-chloroethyl) but-2-enedioate
Molecular Weight
210.06g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2580g/cm3
Interesting facts

Interesting Facts about Bis(2-chloroethyl) But-2-enedioate

Bis(2-chloroethyl) but-2-enedioate is a fascinating compound with a variety of applications in both organic chemistry and industrial processes. Here are some notable aspects:

  • Structure and Reactivity: This compound contains a double bond and two chlorine substituents, which contribute to its unique reactivity. The presence of the but-2-enedioate moiety makes it an interesting target for further chemical transformations.
  • Applications: It is widely used in the production of polymers and can serve as a reagent in organic synthesis. Researchers often explore its potential as a building block for more complex molecules.
  • Toxicity Concerns: Given its structure, bis(2-chloroethyl) but-2-enedioate may pose health risks. Chlorinated compounds are typically associated with carcinogenic properties, making safety measures essential when handling this compound.
  • Historical Significance: The use of chlorinated compounds in chemical warfare during World War I led to increased interest in studies concerning their reactivity and toxicology, including compounds like bis(2-chloroethyl) but-2-enedioate.
  • Research Potential: Ongoing research continues to investigate derivatives of bis(2-chloroethyl) but-2-enedioate, aiming to unlock new applications in medicinal chemistry, such as targeted drug delivery systems.

In summary, bis(2-chloroethyl) but-2-enedioate is not just a compound of interest for its synthetic utility; it also carries a rich history and potential for future research. As scientists endeavor to understand and harness its properties, this compound stands at the crossroads of chemistry, health, and innovation.

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