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Ethyl 2-[(2-diazoacetyl)amino]propanoate

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Identification
Molecular formula
C7H9N3O3
CAS number
. (Placeholder CAS, insert if available)
IUPAC name
ethyl 2-[(2-diazoacetyl)amino]propanoate
State
State

At room temperature, Ethyl 2-[(2-diazoacetyl)amino]propanoate is typically a solid and should be stored in a cool, dry place. It is sensitive to heat and light, with potential for decomposition, so precautions should be taken to minimize exposure to these conditions.

Melting point (Celsius)
93.00
Melting point (Kelvin)
366.15
Boiling point (Celsius)
242.00
Boiling point (Kelvin)
515.15
General information
Molecular weight
198.19g/mol
Molar mass
198.1860g/mol
Density
1.2030g/cm3
Appearence

Ethyl 2-[(2-diazoacetyl)amino]propanoate appears as a yellow or pale orange solid. It may have a crystalline structure depending on its purity and specific preparation method. This compound must be handled with care as diazo compounds are often sensitive to shock or heat.

Comment on solubility

Solubility of Ethyl 2-[(2-diazoacetyl)amino]propanoate

Ethyl 2-[(2-diazoacetyl)amino]propanoate is a fascinating compound with unique solubility characteristics that merit attention. The solubility of this compound can largely be influenced by various factors, including:

  • Polarity: Due to its functional groups, such as the diazoacetyl and amino moieties, the compound exhibits a certain degree of polarity. This can enhance its solubility in polar solvents like water, albeit to a limited extent.
  • Solvent Interaction: The compound may dissolve well in organic solvents such as ethanol, methanol, and acetone, owing to its ethyl ester component.
  • Hydrogen Bonding: The presence of an amino group allows for potential hydrogen bonding with solvent molecules, facilitating solubility in polar environments.

However, it is crucial to note that the solubility may not be extensive. As with many esters, the compound could face limitations based on environmental conditions, such as temperature and pH. In general, compounds with significant structural complexity may show variable solubility, influenced both by their molecular interactions and the nature of the solvent. Thus, empirical testing is often necessary to ascertain the precise solubility profile of ethyl 2-[(2-diazoacetyl)amino]propanoate.

In summary, while ethyl 2-[(2-diazoacetyl)amino]propanoate demonstrates some level of solubility in both polar and nonpolar solvents, the extent remains contingent upon specific conditions and interactions.

Interesting facts

Interesting Facts about Ethyl 2-[(2-diazoacetyl)amino]propanoate

Ethyl 2-[(2-diazoacetyl)amino]propanoate is a fascinating compound that serves as a prime example of how diazo compounds can play important roles in organic chemistry. Here are some notable highlights:

  • Diazo Chemistry: This compound contains a diazo group, which is known for its ability to participate in diverse reactions, including Diazo transfer and azide formation. These reactions are significant in synthesizing complex organic molecules.
  • Biological Importance: Compounds featuring the diazoacetyl functional group may possess biological activity, which fuels interest in their potential uses in pharmaceuticals. Investigating their mechanisms can lead to novel therapeutic agents.
  • Synthetic Utility: Ethyl 2-[(2-diazoacetyl)amino]propanoate can serve as a versatile intermediate in organic synthesis, allowing chemists to create various target molecules through selective transformations.
  • Mechanistic Insights: The study of this compound can provide insights into the reactivity of compounds with amine functionalities and their interactions with electrophiles, which are vital in understanding mechanistic pathways in organic reactions.
  • Environmental Considerations: As scientists explore ways to create more sustainable chemical processes, compounds like this are analyzed for their environmental impact and potential in greener synthesis routes.

In summary, ethyl 2-[(2-diazoacetyl)amino]propanoate is not just a compound of scientific interest due to its structure but also represents a key player in the realms of organic synthesis, pharmaceutical development, and environmental chemistry. The versatility and unique properties of diazo compounds continue to inspire research and innovation in the field.

Synonyms
N-Diazoacetyl-D,L-alanine ethyl ester
819-89-6
CCRIS 925
ALANINE, N-(DIAZOACETYL)-, ETHYL ESTER, D,L-
N-diazoacetyl-dl-alanine ethyl ester