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

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Identification

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
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.

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