(1S,2S)-2-(cyclohexoxy)cyclopropanamine
- Molecular formula
- C9H17NO
- CAS Number
- 129040-68-2
- IUPAC Name
- (1S,2S)-2-(cyclohexoxy)cyclopropanamine
- Molecular Weight
- 153.24g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0365g/cm3
- Synonyms
- trans-(+-)-2-Cyclohexyloxycyclopropylamine
Identification
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.