(1S,2S)-2-(cyclohexoxy)cyclopropanamine

Identification

Molecular formula

C₉H₁₇NO

CAS number

129040-68-2

IUPAC name

(1S,2S)-2-(cyclohexoxy)cyclopropanamine

State

This compound is a liquid at room temperature, possessing a slightly viscous consistency.

Melting point (Celsius)

33.00

Melting point (Kelvin)

306.15

Boiling point (Celsius)

218.00

Boiling point (Kelvin)

491.15

General information

Molecular weight

153.24g/mol

Molar mass

153.2400g/mol

Density

1.0365g/cm³

Appearence

The compound is typically found as a colorless liquid under standard conditions. It may display distinct optical activity due to its chiral centers.

Comment on solubility

Solubility of (1S,2S)-2-(cyclohexoxy)cyclopropanamine

(1S,2S)-2-(cyclohexoxy)cyclopropanamine, a compound characterized by its unique structure, exhibits notable solubility behavior. Understanding its solubility can provide insights into its potential applications in various fields such as pharmaceuticals and organic chemistry.

Key Factors Affecting Solubility

Polar vs. Nonpolar Nature: The compound contains both cyclohexyl (nonpolar) and amino (polar) functional groups, which can influence solubility in polar and nonpolar solvents.
Hydrogen Bonding: The presence of an amino group may facilitate hydrogen bonding with solvents capable of similar interactions, enhancing solubility in polar environments.
Temperature: Increasing temperature often enhances solubility for many compounds; thus, solubility may vary with thermal conditions.

While detailed data on the solubility values for (1S,2S)-2-(cyclohexoxy)cyclopropanamine may be limited, it is generally expected to be:

More soluble in polar solvents (e.g., water or alcohols) due to the inherent polarity of its amino group.
Less soluble in nonpolar solvents (e.g., hydrocarbons) due to the hydrophobic cyclohexyl moiety.

In conclusion, quotably, “The solubility of a compound is crucial for its accessibility and functionality in practical applications.” Thus, further studies are encouraged to elucidate the precise solubility characteristics of (1S,2S)-2-(cyclohexoxy)cyclopropanamine under various conditions.

Interesting facts

Investigating (1S,2S)-2-(cyclohexoxy)cyclopropanamine

(1S,2S)-2-(cyclohexoxy)cyclopropanamine is a fascinating compound that draws attention due to its unique structure and potential applications in medicinal chemistry.

Key Characteristics:

Cyclopropane Ring: The presence of a cyclopropane moiety adds noteworthy strain, which can lead to interesting reactivity patterns.
Chirality: This compound has specific stereochemistry, denoted by the (1S,2S) configuration, which can significantly impact its biological activity and interactions with various biological targets.
Cyclohexoxy Group: The cyclohexoxy substituent is known to impart lipophilicity, enhancing the compound's ability to traverse lipid membranes.

Applications:

This compound's unique features offer intriguing possibilities in several fields:

Pharmaceutical Development: The structural framework could be pivotal in designing new drugs that target neurological or psychiatric conditions.
Organic Synthesis: It may serve as a valuable intermediate in synthetic pathways, paving the way to synthesize more complex molecules.
Research Studies: Its stereochemistry could be extensively studied to reveal more about the relationship between structure and biological function.

Interesting Fact:

As noted by many researchers, "The beauty of cyclopropane derivatives lies in their ability to harness strain for creative reactivity." This means that compounds like (1S,2S)-2-(cyclohexoxy)cyclopropanamine could unlock new avenues for exploration in chemistry!

In conclusion, (1S,2S)-2-(cyclohexoxy)cyclopropanamine exemplifies how even a simple structural modification can lead to profound implications in science and industry.

Synonyms

trans-(+-)-2-Cyclohexyloxycyclopropylamine

5050-97-5

CYCLOPROPYLAMINE, 2-(CYCLOHEXYLOXY)-, trans-(+-)-

DTXSID20964716

2-(Cyclohexyloxy)cyclopropan-1-amine