Dichloroacetyl-DL-serinate sodium

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Identification

Molecular formula
C5H7Cl2NO4Na
CAS Number
25584-83-2
IUPAC Name
sodium;2-[(2,2-dichloroacetyl)amino]-3-hydroxy-propanoate
Molecular Weight
249.02g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2100g/cm3
Interesting facts

Interesting Facts about Sodium; 2-[(2,2-Dichloroacetyl)amino]-3-hydroxy-propanoate

This intriguing compound, also known by its more common name, plays a significant role in various fields of chemistry and biochemistry. Below are some interesting facts that highlight its importance:

  • Versatile Uses: This compound is often utilized in pharmaceutical formulations, showcasing its potential in drug development.
  • Biochemical Significance: Its structure provides a basis for studying amino acids and their derivatives, which are crucial in biological processes.
  • Reactivity: The presence of the 2,2-dichloroacetyl group can make this compound a reactive intermediate, lending it a unique chemistry that can be crucial in synthetic applications.
  • Safety Considerations: Due to the presence of chlorine atoms, proper handling and disposal protocols are essential to minimize potential hazards in laboratory settings.
  • Study of Reactions: This compound serves as a useful subject for exploring acylation reactions, offering insights into the mechanisms of organic synthesis.

As students and researchers dive deeper into the study of sodium; 2-[(2,2-dichloroacetyl)amino]-3-hydroxy-propanoate, they encounter a fascinating blend of organic chemistry and applications in biochemistry. This compound is not just a chemical formula; it embodies a variety of applications and implications that broaden our understanding of chemical interactions in living systems.


In the words of a renowned chemist, "Chemistry is the science of transformations. This compound is a perfect example of how subtle changes in structure can lead to significant implications in reactivity and application."

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