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2-amino-4-imino-1-naphthol

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Identification
Molecular formula
C10H8N2O
CAS number
244-30-6
IUPAC name
2-amino-4-imino-naphthalen-1-one
State
State

At room temperature, 2-amino-4-imino-1-naphthol exists as a solid. It is typically found in crystalline form, indicative of its stable molecular structure. The compound is relatively stable and can maintain its solid state under normal conditions.

Melting point (Celsius)
280.00
Melting point (Kelvin)
553.00
Boiling point (Celsius)
560.00
Boiling point (Kelvin)
833.00
General information
Molecular weight
172.19g/mol
Molar mass
172.1890g/mol
Density
1.3810g/cm3
Appearence

2-Amino-4-imino-1-naphthol typically presents as a crystalline solid. Its appearance can vary from light brown to a darker brown color depending on the purity and specific crystalline form.

Comment on solubility

Solubility of 2-amino-4-imino-naphthalen-1-one

2-amino-4-imino-naphthalen-1-one, a compound with interesting chemical properties, showcases unique solubility characteristics. Its solubility in various solvents can be influenced by several factors:

  • Polarity: The presence of both amino and imino functional groups suggests that 2-amino-4-imino-naphthalen-1-one may demonstrate different solubility profiles in polar versus nonpolar solvents.
  • Hydrogen Bonding: The amino group can engage in hydrogen bonding, which can enhance solubility in polar solvents like water, leading to potential solubility in alcohols as well.
  • Solvent Interaction: The structure allows for interaction with both organic solvents (e.g., dimethyl sulfoxide) and aqueous solutions, possibly indicating moderate to high solubility in these environments.

While detailed solubility data may not be extensively documented, it is generally observed that:

  • Compounds with similar structures tend to show enhanced solubility in polar solvents.
  • Solubility can vary significantly with temperature, and so it may be beneficial to evaluate these properties experimentally.

In conclusion, the solubility of 2-amino-4-imino-naphthalen-1-one is likely to be influenced by its functional groups and the nature of the solvent. To truly grasp its behavior, thorough experimentation in different solvent systems is recommended.

Interesting facts

Interesting Facts about 2-amino-4-imino-naphthalen-1-one

2-amino-4-imino-naphthalen-1-one, also known by its IUPAC name, embodies a rich tapestry of chemical properties and applications that are fascinating to explore. This compound is a derivative of naphthalene, one of the simplest polycyclic aromatic hydrocarbons, and showcases the presence of both amino and imino functional groups, which are significant in organic chemistry.

Chemical Significance

  • Versatile Reactions: The amino group in this compound makes it a potent nucleophile, allowing it to participate in various chemical reactions, such as substitution and condensation reactions.
  • Fluorescence: Naphthalene derivatives are known for their luminescent properties, which may lead to potential applications in the development of fluorescent probes in biological and chemical sensors.
  • Pharmaceutical Applications: Compounds like 2-amino-4-imino-naphthalen-1-one are often investigated for their biological activities, including antimicrobial and antitumor properties, making them candidates for drug development.
  • Complexity in Synthesis: Synthesis of this compound may involve intricate multi-step procedures, showcasing the ingenuity required in synthetic organic chemistry.

Research and Applications

Recent research efforts have focused on:

  • Exploring its role in organic electronics, such as organic light-emitting diodes (OLEDs).
  • Investigating potential reactivity and stability under various conditions, which could provide insights into using these compounds in harsher chemical environments.
  • Using it as a precursor in synthetic pathways to obtain other biologically active molecules.

As a student or scientist, understanding compounds like 2-amino-4-imino-naphthalen-1-one provides valuable insights into the interconnectedness of chemical structures and their functionalities. In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." So, let curiosity lead the way in exploring the diverse landscape of organic compounds!

Synonyms
2-Amino-1,4-naphthoquinone imine
20513-06-8
2-Amino-4-imino-1(4H)-naphthalenone
1(4H)-NAPHTHALENONE, 2-AMINO-4-IMINO-
BRN 2830840
3-14-00-00389 (Beilstein Handbook Reference)
2-amino-4-iminonaphthalen-1-one
2-amino-4-imino-naphthalen-1-one
NSC15013
5438-85-7
1(4H)-Naphthalenone der.
CHEMBL535032
SCHEMBL3273421
1,4-Naphthoquinone imine, 2-amino-