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Carbetapentane

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Identification
Molecular formula
C18H29NO2S
CAS number
77-23-6
IUPAC name
N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid
State
State

At room temperature, carbetapentane is generally found as a liquid.

Melting point (Celsius)
-40.00
Melting point (Kelvin)
233.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
311.49g/mol
Molar mass
311.4850g/mol
Density
1.0613g/cm3
Appearence

Carbetapentane is typically a colorless to light yellow liquid. It is a thick, viscous substance with a slight odor.

Comment on solubility

Solubility Overview

N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid presents interesting characteristics regarding its solubility profile. Understanding the solubility of this compound is crucial for its practical applications in various chemical processes.

Factors Influencing Solubility

The solubility of this compound is influenced by several factors:

  • Polarity: The presence of polar functional groups, such as the carboximidothioic acid moiety, suggests that the compound is likely to be more soluble in polar solvents.
  • Hydrophobic Groups: The isopropoxy group and diethylamino substituents introduce some hydrophobic characteristics, which may decrease its solubility in purely polar solvents.
  • pH Effect: The carboximidothioic acid group can exist in ionized or non-ionized forms depending on the pH of the solution, thereby significantly affecting solubility.

Expected Solubility Characteristics

Based on its structure, we might expect:

  • **Good Solubility in Water**: Particularly at higher pH levels where the compound may become ionized.
  • **Moderate Solubility in Organic Solvents**: Such as alcohols or acetone, due to the presence of hydrophobic portions.
  • Limited Solubility in Nonpolar Solvents: Such as hexane due to its polar functional groups.

In conclusion, the solubility of N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid is a complex interplay of its molecular structure, which must be considered in any chemical application involving this compound. Understanding these solubility traits not only facilitates better handling of the compound but also enhances its efficacy in various scenarios.

Interesting facts

Interesting Facts about N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid

N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid is a fascinating compound due to its unique structural features and versatile applications. Here are some intriguing details about it:

  • Chemical Structure: This compound is notable for its complex molecular framework that includes an aromatic ring, an amine group, and a carboximidothioic acid functionality. Such structural diversity often leads to interesting chemical behavior.
  • Role in Medicinal Chemistry: Compounds like N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid may exhibit significant biological activity, making them valuable in the field of drug discovery. The incorporation of a diethylamino group can enhance solubility and bioavailability.
  • Potential Applications: Beyond medicinal uses, the compound may also be explored in agricultural chemistry, as derivatives of thioic acids are known to exhibit herbicidal properties. This could lead to innovative approaches in pest management.
  • Research Interest: In recent years, compounds containing thioic acid groups have garnered attention for their potential to act as reactants in organic synthesis, aiding in the development of more complex molecules.
  • Safety Considerations: While investigating such compounds, it's vital to conduct thorough safety assessments. Understanding the toxicity and environmental impact of new chemical entities is crucial in modern chemistry.

In summary, N-[2-(diethylamino)ethyl]-4-isopropoxy-benzenecarboximidothioic acid stands as a prime example of how a single compound can open doors to various scientific inquiries and applications, ranging from medicine to agricultural sciences.