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N-(1,2,4-triazol-4-yl)acetamide

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Identification
Molecular formula
C4H6N4O
CAS number
3040-82-4
IUPAC name
N-(1,2,4-triazol-4-yl)acetamide
State
State

At room temperature, N-(1,2,4-triazol-4-yl)acetamide is in a solid state.

Melting point (Celsius)
142.00
Melting point (Kelvin)
415.15
Boiling point (Celsius)
310.00
Boiling point (Kelvin)
583.15
General information
Molecular weight
127.12g/mol
Molar mass
127.1200g/mol
Density
1.3641g/cm3
Appearence

N-(1,2,4-triazol-4-yl)acetamide typically appears as a white crystalline solid. It is known for its relatively simple solid structure, making it identifiable amongst similar chemical compounds.

Comment on solubility

Solubility of N-(1,2,4-triazol-4-yl)acetamide

N-(1,2,4-triazol-4-yl)acetamide is a compound whose solubility plays a vital role in its functionality and application in various fields such as pharmaceuticals and agriculture.

Here are some key points regarding its solubility:

  • Polar Nature: The presence of the triazole ring and the acetamide group contributes to its polar nature, which generally enhances solubility in polar solvents.
  • Solvent Dependence: N-(1,2,4-triazol-4-yl)acetamide is known to be more soluble in water and alcohol compared to non-polar solvents.
  • Hydrogen Bonding: The ability of the acetamide group to participate in hydrogen bonding further promotes solubility in polar environments.
  • Temperature Influence: Like many organic compounds, solubility may increase with temperature, which can be an important consideration for practical applications.

In conclusion, the solubility of N-(1,2,4-triazol-4-yl)acetamide in various solvents is heavily influenced by its structural characteristics, making it an interesting compound for study and application. As always, experimenting with different conditions will yield the best understanding of its solubility behavior in the intended medium.

Interesting facts

Interesting Facts about N-(1,2,4-triazol-4-yl)acetamide

N-(1,2,4-triazol-4-yl)acetamide is a fascinating organic compound that belongs to the class of triazole derivatives. This compound is notable for several reasons:

  • Pharmaceutical Significance: The triazole ring in this compound is known for its *antifungal* properties, making it a critical component in the synthesis of various pharmaceuticals, particularly in the treatment of fungal infections.
  • Research Applications: Scientists often explore triazole derivatives for their potential in *agricultural* applications, such as crop protection and enhancing resistance to diseases.
  • Chemical Versatility: The functional groups present in N-(1,2,4-triazol-4-yl)acetamide enable it to act as a versatile building block in organic synthesis, facilitating the creation of a wide range of other useful compounds.
  • Biological Activity: Research indicates that this compound exhibits various biological activities, including *antimicrobial*, *anti-inflammatory*, and potential *anticancer* effects, making it a subject of interest in medicinal chemistry.

As noted by chemists, "The triazole backbone provides a unique scaffold that leads to a diverse array of biological activities." This compound is a prime example of how small structural modifications can significantly impact *biological efficacy* and *chemical reactivity*.

In summary, N-(1,2,4-triazol-4-yl)acetamide embodies the intersection of chemistry and biology, where its unique structure has implications in both medicinal and agricultural fields. Its study opens up avenues for developing innovative therapies and solutions to pressing biological challenges.

Synonyms
AKOS003864406