N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine

Identification

Molecular formula

C₂₀H₂₄Cl₂N₂

CAS number

74793-33-6

IUPAC name

N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine

State

At room temperature, N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine is generally encountered as a liquid, which is due to its relatively low melting point just above room temperature.

Melting point (Celsius)

15.20

Melting point (Kelvin)

288.35

Boiling point (Celsius)

248.60

Boiling point (Kelvin)

521.75

General information

Molecular weight

384.28g/mol

Molar mass

384.2760g/mol

Density

1.1374g/cm³

Appearence

N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine is typically a colorless to pale yellow liquid. It may appear slightly thick due to its molecular structure.

Comment on solubility

Solubility of N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine

N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine is a unique chemical compound with distinct solubility characteristics. The aromatic nature of its structure, particularly the presence of chlorophenyl groups, greatly influences its solubility in various solvents. Here are key points regarding its solubility:

Solvent Polarity: The solubility of this compound is significantly affected by the polarity of the solvent. It tends to be more soluble in non-polar solvents such as hexane and toluene.
Water Solubility: Its solubility in water is quite limited due to the hydrophobic alkyl and aromatic components, contributing to its overall low water solubility.
Temperature Effects: Generally, increasing the temperature can enhance solubility in organic solvents, though the effect in water remains marginal.
Influence of Substituents: The presence of chlorine substituents impacts the compound's electronic characteristics, potentially leading to varied solubility in different solvent environments.

To summarize, while N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine demonstrates greater solubility in non-polar organic solvents, it proves to be relatively insoluble in water and polar solvents, making studies of its behavior or applications particularly interesting. The interplay of its structural features and solvent properties lays the groundwork for further exploration in chemical applications.

Interesting facts

Interesting Facts about N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine

N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine is a fascinating compound that showcases the complex interactions between molecular structure and biological activity. Here are some noteworthy points:

Dual Functionality: This compound not only has amine functionalities but also contains chlorophenyl groups, which are known to enhance the compound's reactivity and provide potential applications in medicinal chemistry.
Structure-Activity Relationship: The presence of chlorine on the phenyl ring can significantly alter the biological properties of this compound, making it a subject of interest for drug design and development.
Potential Applications: Compounds like this one are often explored for their potential as antibacterial or antifungal agents due to their unique structural properties.
Versatile Reactivity: The amine groups in this molecule can participate in a variety of chemical reactions including nucleophilic substitution and acylation, which may lead to the synthesis of novel derivatives.

As quoted by a renowned chemist, "Understanding the subtleties of molecular interactions can unlock new frontiers in pharmaceuticals." This statement resonates well with compounds like N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine, underscoring its potential in advancing medicinal chemistry.

In summary, the study of N,N'-bis[(2-chlorophenyl)methyl]hexane-1,6-diamine provides an excellent opportunity to explore the delicate balance between structure and function, revealing insights that could lead to innovative applications in various scientific fields.