Allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate

Identification

Molecular formula

C₂₄H₃₅NO₂

CAS number

.n.a

IUPAC name

allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate

State

At room temperature, Allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate is usually in a liquid state. It might exhibit slight viscosity and is clear to light yellow in appearance.

Melting point (Celsius)

-15.00

Melting point (Kelvin)

258.15

Boiling point (Celsius)

347.00

Boiling point (Kelvin)

620.15

General information

Molecular weight

353.51g/mol

Molar mass

353.5140g/mol

Density

1.0500g/cm³

Appearence

The compound is typically a colorless to pale yellow liquid. It may have a characteristic odor. The liquid is clear and free-flowing, with no particulate matter or cloudiness.

Comment on solubility

Solubility of Allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate

The solubility of allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate can be quite intriguing due to its complex structure. This organic compound is characterized by the presence of both polar and nonpolar functional groups which influence its solubility behavior in various solvents. Here are some important points about its solubility:

Polar vs Nonpolar: Given the dimethylamino group, this compound exhibits some polar characteristics, which may enhance its solubility in polar solvents like water. However, the presence of the bulky naphthyl and isopropyl groups contributes to significant hydrophobic character, making it less soluble in water.
Solvent Interaction: This compound is likely to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane, where the nonpolar parts of the molecule interact favorably with the solvent molecules.
Temperature Dependence: Like many organic compounds, its solubility can be temperature-dependent. Generally, increasing the temperature can enhance solubility in organic liquids.
Concentration Effects: Be aware of the concentration level; at higher concentrations, precipitation may occur in less miscible solvents due to saturation limits.

In summary, the solubility of allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate is a reflection of its unique structural features, making it soluble in organic solvents while presenting challenges in aqueous environments. As a general guideline, **polarities and solvent types** play crucial roles in determining the solubility profiles of this compound.

Interesting facts

Interesting Facts about Allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate

Allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate is a fascinating compound that showcases the interplay of various chemical functionalities. This compound is an example of how small changes in molecular structure can lead to significant variations in properties and biological activities. Here are some intriguing insights:

Structure-Activity Relationship: The presence of the dimethylamino group in its structure indicates potential for interaction with biological systems, often enhancing the compound's activity. This characteristic makes the study of such molecules crucial in medicinal chemistry.
Flavor and Fragrance Applications: Compounds with similar structures are often found in flavor and fragrance industries, allowing researchers and chemists to explore synthetic pathways to create novel scents and tastes.
Potential Use in Synthesis: The allyl group in this compound is known for its reactivity, particularly in various organic reactions such as allylic substitutions, making it a valuable intermediate in organic synthesis.
Research Applications: Due to its unique structure, this compound may serve as a model in pharmacological studies, especially in exploring newly defined targets for drug discovery.

As stated by renowned chemist, "The beauty of organic chemistry lies in the complexity that can arise from simple building blocks." This compound exemplifies that idea, bridging various chemical realms and piquing the interest of chemists and researchers alike.

Overall, the study of allyl 5-(dimethylamino)-2-isopropyl-2-(1-naphthyl)pentanoate not only enhances our understanding of chemical bonding but also opens doors to innovative applications in medicine, flavoring, and synthesis.

Synonyms

14938-54-6

prop-2-enyl 5-(dimethylamino)-2-naphthalen-1-yl-2-propan-2-ylpentanoate

alpha-(3-(Dimethylamino)propyl)-alpha-isopropyl-1-naphthaleneacetic acid allyl ester

alpha-[3-(Dimethylamino)propyl]-alpha-isopropyl-1-naphthaleneacetic acid allyl ester

BRN 2770948

1-Naphthaleneacetic acid, alpha-(3-(dimethylamino)propyl)-alpha-isopropyl-, allyl ester

DTXSID30933635

prop-2-en-1-yl 5-(dimethylamino)-2-(naphthalen-1-yl)-2-(propan-2-yl)pentanoate