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N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide

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Identification
Molecular formula
C6H6N6O2
CAS number
199688-94-9
IUPAC name
N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide
State
State

The compound is usually found in a solid state at room temperature.

Melting point (Celsius)
246.50
Melting point (Kelvin)
519.65
Boiling point (Celsius)
487.30
Boiling point (Kelvin)
760.45
General information
Molecular weight
204.18g/mol
Molar mass
204.1760g/mol
Density
1.4120g/cm3
Appearence

This compound typically appears as a solid, however, detailed descriptions of its color and texture may vary depending on its purity and other specific conditions of observation.

Comment on solubility

Solubility of N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide

N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide demonstrates varied solubility characteristics in different solvents, attributing to its complex molecular structure. Understanding its solubility can provide valuable insight into its applicability in various chemical processes.

Key Solubility Information:

  • Polar Solvents: Generally exhibits good solubility in polar solvents such as dimethyl sulfoxide (DMSO) and water due to the presence of hydrophilic amino and carbonyl functional groups.
  • Non-Polar Solvents: Shows limited solubility in non-polar solvents like hexane or benzene, which can be attributed to the lack of appropriate interactions between the compound and these solvents.
  • Temperature Effect: Solubility may increase with temperature in polar solvents, facilitating greater interaction and dissolution.

In summary, N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide is a compound whose solubility is heavily influenced by solvent polarity and temperature. Its ability to dissolve in certain solvents underscores its potential use in various chemical applications, from pharmaceuticals to organic synthesis.

Interesting facts

Exploring N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide

N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide is a fascinating compound gaining attention in the fields of medicinal chemistry and biochemistry. Here are some intriguing insights about this compound:

  • Unique Structure: The compound contains a pyrazolo moiety fused with a triazine ring, contributing to its unique biological activity.
  • Potential Therapeutic Applications: Due to its structural characteristics, it is being studied for its potential as an antitumor agent, showcasing the ability to inhibit specific cellular pathways.
  • Research Significance: The synthesis of this compound can help in understanding the interactions of heterocyclic compounds, which are crucial in drug development.
  • Analytical Interest: Its complex chemical structure offers a rich platform for various analytical techniques, including NMR and mass spectrometry, which can unveil deeper insights into its reactivity and stability.

The reaction mechanisms involving this compound are also of particular interest:

  1. It may undergo substitution reactions due to the presence of the amino group, which can donate electrons.
  2. The carbonyl group in the structure can make the compound more reactive toward nucleophiles.

As we delve into the world of chemical compounds like N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide, we are reminded of the vast potential these molecules have in shaping future therapeutic strategies. It's exciting to imagine the breakthroughs that compounds with such intricate structures can bring forth in the healthcare realm!

Synonyms
16111-79-8
DTXSID20167068
N-((4-Aminopyrazolo(5,1-c)(1,2,4)triazine-3-carbonyl)amino)formamide
N-[(4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbonyl)amino]formamide
DTXCID6089559
N/'-Formyl-4-aminopyrazolo[5,1-c][1,2,4]triazine-3-carbohydrazide
XNSHTOSUNFBYOQ-UHFFFAOYSA-N
Hydrazine, 1-[(4-aminopyrazolo[5,1-c]-as-triazin-3-yl)carbonyl]-2-formyl-
4-Amino-N'-formylpyrazolo[5,1-c][1,2,4]triazine-3-carbohydrazide #