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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
State
State

At room temperature, it is a solid compound.

Melting point (Celsius)
162.00
Melting point (Kelvin)
435.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
249.02g/mol
Molar mass
249.0200g/mol
Density
1.2100g/cm3
Appearence

The compound appears as a white crystalline powder.

Comment on solubility

Solubility of Sodium 2-[(2,2-Dichloroacetyl)amino]-3-hydroxy-propanoate

The solubility of sodium 2-[(2,2-dichloroacetyl)amino]-3-hydroxy-propanoate is an intriguing topic due to its unique structural features. In aqueous solutions, several factors play a critical role in determining its solubility:

  • Ionic Nature: Being a sodium salt, its ionic functionalities often enhance solubility in water.
  • Polarity: The polar nature of the hydroxy and amino groups can promote solvation, leading to favorable interactions with water molecules.
  • Temperature Influence: Generally, solubility may increase with temperature; thus, heating the solution might enhance the solubility rate.
  • pH Levels: The solubility can also be affected by the pH of the solution, as the protonation states of the amino group can alter solubility characteristics.

It is often observed that compounds structured similarly tend to have varying degrees of solubility based on these parameters. For sodium 2-[(2,2-dichloroacetyl)amino]-3-hydroxy-propanoate, one could state:

"The presence of sodium enhances its ability to dissolve in polar solvents like water, while the specific functional groups contribute both positively and negatively to overall solubility."

In summary, while this compound is expected to have a reasonable solubility in water due to the ionic and polar characteristics, experimental data would provide a more definitive understanding of its solubility profile.

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."