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Ethyl diazoacetate

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Identification
Molecular formula
C4H6N2O2
CAS number
623-73-4
IUPAC name
ethyl 2-[(2-diazoacetyl)amino]acetate
State
State

At room temperature, ethyl diazoacetate is a liquid.

Melting point (Celsius)
-23.00
Melting point (Kelvin)
250.15
Boiling point (Celsius)
141.50
Boiling point (Kelvin)
414.65
General information
Molecular weight
128.10g/mol
Molar mass
128.0990g/mol
Density
1.1625g/cm3
Appearence

Ethyl diazoacetate is a yellow to orange liquid with a pungent odor. It is light-sensitive and tends to decompose explosively under heat or shock. It must be handled with care due to its potential explosiveness.

Comment on solubility

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

The solubility of ethyl 2-[(2-diazoacetyl)amino]acetate is an intriguing aspect to consider, particularly due to its unique structure and functional groups. Here are some key points regarding its solubility:

  • Polarity: The presence of polar groups, such as the amine and carbonyl functionalities, suggests that the compound may exhibit moderate solubility in polar solvents like water.
  • Solvent Interaction: The molecule's structure indicates that it could potentially form hydrogen bonds with solvents, thereby enhancing its solubility in polar environments.
  • Non-Polar Solvents: Conversely, the ethyl group could result in lower solubility in non-polar solvents, due to reduced interactions with these types of solvents.
  • Temperature Effects: As with many organic compounds, solubility may vary significantly with temperature, often increasing in warmer environments.
  • Concentration Thresholds: It is crucial to consider the concentration limits when dissolving in solvents; exceeding these may lead to precipitation.

In summary, while ethyl 2-[(2-diazoacetyl)amino]acetate shows promise for solubility in a range of environments, its behavior will greatly depend on the solvent type and environmental conditions. Investigating these factors can yield important insights into its practical applications.

Interesting facts

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

Ethyl 2-[(2-diazoacetyl)amino]acetate is a fascinating chemical compound that finds its place within the realm of synthetic chemistry and organic reactions. Here are some intriguing aspects to consider:

  • Reactivity: This compound contains a diazo group, which is known for its ability to participate in various chemical reactions, including click chemistry and cycloaddition reactions. This reactivity opens doors for creating complex structures in organic synthesis.
  • Applications: Ethyl 2-[(2-diazoacetyl)amino]acetate can serve as a versatile building block in the preparation of pharmaceuticals and biologically active molecules. Its unique structure may lead to novel drug candidates in medicinal chemistry.
  • Research Potential: Ongoing studies explore the use of diazo compounds in materials science, particularly in the synthesis of polymers with specific properties. This compound might pave the way for advancements in material design.
  • Chemical Warfare Agents: While not directly associated with harmful uses, its diazo component puts it amongst compounds that require careful handling. This emphasizes the importance of safety and regulation in chemical research.
  • Historical Context: Diazo compounds have a rich history in the field of chemistry, dating back to the late 19th century when they were first studied. They are often used in dye manufacturing, showcasing their significance in industrial applications.

In summary, ethyl 2-[(2-diazoacetyl)amino]acetate is not just a compound with a complex name but a significant player in the world of synthetic chemistry, with potential implications in various domains such as medicine and materials science. As researchers continue to unlock the mysteries of compounds like this, we may soon discover even more remarkable applications.

Synonyms
Diazoacetylglycine ethyl ester
999-29-1
N-Diazoacetylglycine ethyl ester
O-Ethyl N-diazoacetylglycine
M 405
Z9Z37Y830Q
NSC-58406
ethyl 2-((2-diazoacetyl)amino)acetate
Ethyl diazoacetylglycinate
CCRIS 928
NSC 58406
UNII-Z9Z37Y830Q
AI3-52379
GLYCINE, N-(DIAZOACETYL)-, ETHYL ESTER
N-(Diazoacetyl)glycine ethyl ester
diazoacetylglycine ethylester
DTXSID30878936
NSC58406
ETHYL N-DIAZOACETYLGLYCINE, O-
N-DIAZOACETYLGLYCINE,ETHYL ESTER
Q27295195