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2-Chloro-3-(sec-butylamino)naphthalene-1,4-dione

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Identification
Molecular formula
C14H14ClNO2
CAS number
Not available
IUPAC name
2-chloro-3-(sec-butylamino)naphthalene-1,4-dione
State
State

At room temperature, 2-Chloro-3-(sec-butylamino)naphthalene-1,4-dione is typically found in a solid state. The compound is a fine crystalline powder that is stable under standard conditions.

Melting point (Celsius)
112.50
Melting point (Kelvin)
385.70
Boiling point (Celsius)
378.50
Boiling point (Kelvin)
651.70
General information
Molecular weight
283.72g/mol
Molar mass
283.7460g/mol
Density
1.3580g/cm3
Appearence

The compound appears as a crystalline solid, typically exhibiting a distinct color ranging from light yellow to a yellow-brown hue. Its crystalline nature gives it a shiny, reflective appearance which is evident under proper lighting conditions.

Comment on solubility

Solubility of 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione

The solubility of 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione presents an intriguing case for study. This compound, which contains both aromatic and amine functionalities, often demonstrates variable solubility in different environments.

Factors Influencing Solubility

The solubility of this compound can be influenced by several key factors:

  • Polarity: The presence of polar functional groups may enhance solubility in polar solvents such as water or ethanol.
  • Hydrophobic Interactions: The naphthalene structure contributes to hydrophobic characteristics, which may limit solubility in highly polar solvents.
  • Temperature: Increasing temperature typically enhances solubility for solid compounds.
  • pH of the Solution: The ionization of the amine group can vary with pH, affecting solubility in aqueous environments.

General Observations

In practice, it is often noted that:

  • This compound is likely to be more soluble in organic solvents like dimethyl sulfoxide (DMSO) or ethanol due to their compatibility with aromatic systems.
  • Its solubility in water is expected to be limited, typically indicating a medium to low solubility level.

As with many organic compounds, experimentation may yield the most reliable insights into the solubility behavior of 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione. Always refer to specific experimental conditions for precise solubility data.

Interesting facts

Interesting Facts about 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione

2-chloro-3-(sec-butylamino)naphthalene-1,4-dione is a fascinating organic compound that belongs to the class of naphthalene derivatives, which are known for their complex structures and a wide variety of biological activities. Here are some intriguing aspects of this compound:

  • Biological Significance: Compounds similar to 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione often exhibit potent biological properties, making them of great interest in pharmaceutical research. They can act as potential *anti-cancer*, *anti-inflammatory*, or *antimicrobial* agents.
  • Structural Diversity: This compound features a naphthalene core, which gives it unique electronic properties. The substitution of chlorine and the sec-butylamino group significantly influences its reactivity and interaction with biological targets, illustrating the importance of molecular substituents in organic chemistry.
  • Synthesis Routes: The synthesis of this compound often involves complex organic reactions. Understanding the steps required for its synthesis allows chemists to explore various methods of functionalizing aromatic compounds, enriching their toolbox for creating diverse chemical architectures.
  • Environmental Impact: As a derivative of naphthalene, the environmental behavior of compounds like 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione is an area of ongoing research. Studies may focus on their degradation pathways and the potential impacts of chlorinated compounds on ecology, especially in urban settings.

In conclusion, 2-chloro-3-(sec-butylamino)naphthalene-1,4-dione serves as a striking example of the intersection of organic chemistry and pharmacology. Its unique structural features not only enhance its biological potential but also open avenues for innovative research in various chemical disciplines.

Synonyms
22272-32-8
2-sec-Butylamino-3-chloro-1,4-naphthoquinone
1,4-NAPHTHOQUINONE, 2-(sec-BUTYLAMINO)-3-CHLORO-
NSC 91103
BRN 3093349
NSC91103
RefChem:1053339
1, 2-(sec-butylamino)-3-chloro-
NSC-91103
WLN: L66 BV EVJ CMY2&1 DG
DS-008456
1,4-Naphthalenedione,2-chloro-3-[(1-methylpropyl)amino]-