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Pyrithyldione

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Identification
Molecular formula
C15H20BrN3
CAS number
32444-19-2
IUPAC name
N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine
State
State

At room temperature, pyrithyldione exists as a solid. It is known for its stability and resistance to changes in environmental conditions.

Melting point (Celsius)
118.00
Melting point (Kelvin)
391.15
Boiling point (Celsius)
400.00
Boiling point (Kelvin)
673.15
General information
Molecular weight
333.25g/mol
Molar mass
333.2500g/mol
Density
1.3400g/cm3
Appearence

Pyrithyldione typically appears as a crystalline solid that is white or off-white in color.

Comment on solubility

Solubility of N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine

This compound, with its complex structure, exhibits unique solubility characteristics that can be influenced by various factors. Understanding its solubility is vital for applications in both biological and chemical processes.

Factors Affecting Solubility

The solubility of N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine can be affected by:

  • Polarity: The presence of the polar pyridyl group and the amine functionalities generally increases solubility in polar solvents.
  • Temperature: Solubility often increases with temperature, making it significant in thermodynamic studies.
  • pH Levels: This compound may behave differently across various pH levels due to the presence of basic amine groups, which can become protonated.
  • Solvent Type: It tends to dissolve better in organic solvents such as DMSO or DMF compared to water due to its hydrophobic regions influenced by the bromophenyl moiety.

General Observations

In general, one might expect:

  • Higher solubility in organic solvents compared to aqueous solutions.
  • Temperature increases can enhance solubility, particularly in organic media.
  • Possible variable solubility due to interactions with other chemical species.

To summarize, while N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine displays distinctive solubility traits, further experimental data would provide a clearer understanding of its behavior under varying conditions. Understanding these solubility dynamics is crucial for its application in pharmaceuticals and chemical synthesis.

Interesting facts

Interesting Facts about N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine

N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine is a remarkable compound that exhibits fascinating properties and applications in various fields of chemistry. Here are some noteworthy aspects:

  • Pharmaceutical Potential: This compound is of significant interest in medicinal chemistry. Its structure, which includes a pyridine ring and a bromophenyl group, can contribute to its biological activity, making it a potential candidate for drug development.
  • Ligand Properties: Due to its nitrogen-containing functional groups, this compound can act as a ligand in coordination chemistry. It is capable of forming complexes with transition metals, which are vital in catalysis and material science.
  • Research Applications: The unique moieties in the structure allow for various modifications that can lead to the synthesis of new derivatives. Researchers often explore these derivatives to enhance biological activity or alter chemical properties.
  • Synthetic Versatility: The synthesis of N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine can be accomplished through different pathways. This versatility makes it an attractive compound for experimental chemists who are looking to innovate.
  • Importance in Organic Synthesis: The presence of both amine and pyridine groups highlights its importance in organic synthesis. Such compounds are commonly utilized as building blocks for constructing complex organic molecules.

In conclusion, N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-(2-pyridyl)ethane-1,2-diamine not only serves as a fascinating example of a chemically rich compound but also emphasizes the interdisciplinary nature of modern chemistry. As *scientists* continue to explore its properties, the potential for groundbreaking discoveries remains vast.

Synonyms
Hibernon
531-09-9
N'-[(4-bromophenyl)methyl]-N,N-dimethyl-N'-pyridin-2-ylethane-1,2-diamine
4-Bromtripelennamin
BRN 0257088
SCHEMBL8386885
2-((p-Bromobenzyl)(2-(dimethylamino)ethyl)amino)pyridine
DTXSID20201178
N-(4-Brombenzyl)-N',N'-dimethyl-N-(2-pyridyl)ethylendiamin
Pyridine, 2-((p-bromobenzyl)(2-(dimethylamino)ethyl)amino)-
N-(p-Bromobenzyl)-N',N'-dimethyl-N-(2-pyridyl)ethylenediamine
Ethylenediamine, N-(p-bromobenzyl)-N',N'-dimethyl-N-(2-pyridyl)-
1,2-Ethanediamine, N-((4-bromophenyl)methyl-N',N'-dimethyl-N-2-pyridinyl-