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Triazenemelamine

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Identification
Molecular formula
C12H15Cl2N7
CAS number
57149-07-2
IUPAC name
N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine
State
State

At room temperature, Triazenemelamine is typically found in a solid state.

Melting point (Celsius)
162.00
Melting point (Kelvin)
435.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
348.21g/mol
Molar mass
348.2090g/mol
Density
1.5760g/cm3
Appearence

Triazenemelamine typically appears as a crystalline solid that can vary in color from white to slightly off-white. The exact appearance may vary depending on the purity and form of the compound.

Comment on solubility

Solubility of N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine

The solubility of N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine can be a complex subject due to its unique chemical structure and characteristics. Here are some key points to consider:

  • Solvent Interaction: This compound may demonstrate variable solubility depending on the solvent used. It is generally expected to have better solubility in polar solvents due to the presence of amine groups.
  • Temperature Effect: Solubility often increases with temperature; thus, heating the solution may enhance the dissolution of this compound.
  • pH Dependence: As an amine-containing compound, its solubility can also be affected by the pH of the solution, potentially resulting in improved solubility in acidic conditions.

To summarize, although the specific solubility characteristics for this compound may not be extensively cataloged, understanding the variables that influence solubility is crucial. It can be beneficial to test solubility experimentally in various solvents and conditions to appreciate fully the behavior of N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine in practical applications.

Interesting facts

Interesting Facts About N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine

N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine is a notable compound within the realm of chemical research and development, particularly due to its potential applications and unique properties. Here are some fascinating insights:

  • Versatile Applications: This compound has garnered attention in medicinal chemistry, particularly in the design of pharmaceutical agents aimed at treating various diseases, including cancer and infectious diseases.
  • Triazole Ring: The presence of a triazole structure in its molecular framework contributes not only to its chemical stability but also enhances its biological activity. Triazoles are known for their antifungal and antimicrobial properties, making them invaluable in drug design.
  • Chloroethyl Groups: The bis(2-chloroethyl)amino moiety is significant for its alkylating properties, which can disrupt DNA synthesis in rapidly dividing cells—a mechanism often leveraged in cancer therapies.
  • Research Potential: Ongoing studies are exploring the combinatorial approaches in which this compound might serve as a critical building block for novel therapeutic agents, possibly leading to more effective treatment options.
  • Synthesis Challenges: The synthesis of such complex compounds often involves multi-step reaction processes, which require precision and careful optimization to yield the desired products with high purity.

As we continue to explore the profound implications of N3-[[4-[bis(2-chloroethyl)amino]phenyl]methyleneamino]-1,2,4-triazole-3,4-diamine, it reminds us of the intricate relationship between chemistry and medicine, leading to groundbreaking advancements that can significantly impact human health.

Synonyms
NCIOpen2_008971