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2-Chloro-3-methoxy-1,4-naphthoquinone

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Identification
Molecular formula
C11H7ClO3
CAS number
82-15-1
IUPAC name
2-chloro-3-methoxy-naphthalene-1,4-dione
State
State

At room temperature, 2-Chloro-3-methoxy-1,4-naphthoquinone is typically found in a solid state. Its crystalline nature is often observed in solid samples, making it stable under standard conditions.

Melting point (Celsius)
108.00
Melting point (Kelvin)
381.10
Boiling point (Celsius)
312.10
Boiling point (Kelvin)
585.30
General information
Molecular weight
222.62g/mol
Molar mass
222.6160g/mol
Density
1.5712g/cm3
Appearence

2-Chloro-3-methoxy-1,4-naphthoquinone typically appears as a yellow crystalline solid. This compound is known for its bright color and distinct crystalline form, making it recognizable in laboratory settings.

Comment on solubility

Solubility of 2-Chloro-3-Methoxy-Naphthalene-1,4-Dione

2-Chloro-3-methoxy-naphthalene-1,4-dione, a substituted naphthoquinone, exhibits notable characteristics regarding its solubility. Understanding the solubility of this compound is crucial for applications in various fields including organic synthesis and materials science.

Solubility Characteristics:

  • Solvent Dependency: The solubility of 2-chloro-3-methoxy-naphthalene-1,4-dione is highly dependent on the choice of solvent. It tends to dissolve well in polar organic solvents such as acetone and ethanol.
  • Water Solubility: The compound is sparingly soluble in water, which limits its applications in aqueous environments. This is predominantly due to its hydrophobic aromatic structure.
  • Temperature Influence: Like many organic compounds, its solubility can increase with temperature. Higher temperatures facilitate better solvation dynamics, improving dissolving rates.
  • Complexations: In some cases, it can form complexes with certain metals, which can affect its solubility characteristics in specific environments.

In conclusion, the solubility of 2-chloro-3-methoxy-naphthalene-1,4-dione is essential to consider when utilizing it in practical applications. Its moderate solubility in polar solvents makes it valuable for chemical reactions and processes, while its limited water solubility might constrain its usage in biological systems.

Interesting facts

Interesting Facts about 2-Chloro-3-methoxy-naphthalene-1,4-dione

2-Chloro-3-methoxy-naphthalene-1,4-dione is a fascinating compound with a variety of interesting attributes. This compound belongs to a class of chemicals known as naphthoquinones, which are distinguished by their significant role in biological and synthetic processes. Here are some intriguing facts about 2-chloro-3-methoxy-naphthalene-1,4-dione:

  • Biosynthetic Importance: Naphthoquinones like this one are significant in the biosynthesis of various natural products, such as pigments and electron carriers in plants.
  • Pharmacological Properties: Compounds related to naphthoquinones have shown antimicrobial and anticancer properties, making them subjects of extensive research in medicinal chemistry.
  • Versatile Reactivity: The presence of the chloro group in 2-chloro-3-methoxy-naphthalene-1,4-dione enhances its reactivity, enabling it to participate in various chemical reactions, including electrophilic substitutions and nucleophilic attacks.
  • Applications in Dyes: Naphthoquinone derivatives often find their way into dye manufacturing; they can act as intermediates in the production of vivid organic pigments for textiles and art materials.
  • Photochemistry: This compound may exhibit interesting photochemical properties, making it a candidate for studies involving light and its interaction with organic compounds.

In addition to its chemical fascinating aspects, the study of 2-chloro-3-methoxy-naphthalene-1,4-dione serves as a gateway to understanding the broader characteristics of structural modifications in naphthoquinones. As Albert Szent-Györgyi, the Nobel Prize-winning biochemist, once said, "Discovery consists of seeing what everybody has seen and thinking what nobody has thought." The study of such compounds can reveal innovative approaches to tackling various scientific challenges.

This compound showcases the beautiful complexity of organic chemistry, exhibiting a blend of reactivity, utility, and biological significance that captivates scientists and students alike.

Synonyms
2-Chloro-3-methoxy-1,4-naphthoquinone
15707-32-1
1,4-NAPHTHOQUINONE, 2-CHLORO-3-METHOXY-
2-chloro-3-methoxynaphthalene-1,4-dione
NSC 4260
BRN 2262276
NSC4260
CHEMBL350242
SCHEMBL8285443
DTXSID50166206
2-Chloro-3-methoxynaphthoquinone #
NSC-4260
2-methoxy-3-chloro-1,4-naphthoquinone
3-chloro-2-methoxy-1,4-naphtho-quinone
3-Chloro -2-methoxy-1,4-naphthoquinone
1,4-Naphthoquinone, 2-chloro-3-metho xy-
1,4-Naphthalenedione, 2-chlo ro-3-methoxy-