(4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium chloride

Identification

Molecular formula

C₂₂H₃₆ClNO

IUPAC name

(4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride

State

At room temperature, (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium chloride is typically found in a solid state.

Melting point (Celsius)

45.00

Melting point (Kelvin)

318.15

Boiling point (Celsius)

230.00

Boiling point (Kelvin)

503.15

General information

Molecular weight

398.99g/mol

Molar mass

398.9890g/mol

Density

1.0421g/cm³

Appearence

The compound appears as a white crystalline solid.

Comment on solubility

Solubility of (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride

The solubility of the compound (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride can be understood through various factors that influence how well it dissolves in different solvents. Here are some key points regarding its solubility:

Polarity: The presence of ionic ammonium groups indicates that this compound may have a certain degree of polarity, which generally enhances solubility in polar solvents, such as water.
Hydrophobicity: The heptoxynaphthalene portion of the compound consists of a hydrophobic aromatic system that may limit solubility in water but promote solubility in organic solvents.
Solvent Interactions: Depending on the solvent, the degree of solubility can vary significantly:
- Polar solvents: Expected to dissolve the ammonium chloride portion effectively.
- Non-polar solvents: May favor the aromatic structure, enhancing solubility in organic media.
Temperature: Solubility often increases with temperature; thus, heating may improve the dissolution of this compound in various solvents.

In summary, the solubility of (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride is a complex interplay of its structural characteristics and the nature of the solvent. *Understanding these interactions is crucial for predicting its behavior in practical applications.*

Interesting facts

Exploring (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride

This intriguing compound, with its lengthy and complex name, belongs to the category of ammonium salts. It serves as a fascinating subject within the realm of organic chemistry due to its unique structure and potential applications.

Key Characteristics

Ammonium Salt: The presence of the diisopropylammonium moiety suggests this compound can function effectively in various chemical reactions, making it an ideal candidate for a wide range of applications.
Functional Groups: The naphthalene and carboximidoyl components indicate this compound could participate in interesting reactions due to the reactivity of the imido group, thus holding potential within synthetic organic chemistry.
Therapeutic Potential: Compounds similar to this have been explored for their biological activity, hinting at potential applications in pharmaceuticals or materials science.

Interesting Insights

One of the most noteworthy aspects of this compound is its molecular framework. The integration of a naphthalene ring with a heptoxy substituent not only enhances the stability of the structure but also contributes to its *lipophilicity*. This unique feature is advantageous for drug delivery systems, allowing for better solubility in biological membranes.

Furthermore, synthesizing compounds like (4-heptoxynaphthalene-1-carboximidoyl)-diisopropyl-ammonium;chloride can also encourage the exploration of diverse chemical pathways, leading to the discovery of new materials and reactants.

As stated by eminent chemists, "The complexity of a molecule often reflects its potential utility." This compound is a testament to that principle, inspiring further research and experimentation in chemical synthesis and medicinal chemistry.

Synonyms

N,N-Diisopropyl-4-heptyloxy-1-naphthamidine hydrochloride

1-NAPHTHAMIDINE, N,N-DIISOPROPYL-4-HEPTYLOXY-, MONOHYDROCHLORIDE

22824-42-6

RefChem:1056028