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CAS 213764-26-2

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(1R,2S)-2-Aminocyclohexanemethanol

Description:
(1R,2S)-2-Aminocyclohexanemethanol is a chiral amine characterized by its cyclohexane ring structure, which features an amino group and a hydroxymethyl group attached to the second carbon of the ring. This compound exhibits both basic and nucleophilic properties due to the presence of the amino group, making it useful in various chemical reactions, including those in organic synthesis and medicinal chemistry. The specific stereochemistry indicated by the (1R,2S) configuration suggests that it has distinct spatial arrangements that can influence its biological activity and interactions with other molecules. As a secondary amine, it can participate in hydrogen bonding, which may enhance its solubility in polar solvents. Additionally, the presence of the hydroxymethyl group can contribute to its reactivity and potential applications in the development of pharmaceuticals or as a building block in organic synthesis. Overall, (1R,2S)-2-Aminocyclohexanemethanol is a versatile compound with significant implications in both research and industrial applications.
Formula:C7H15NO
InChI:InChI=1S/C7H15NO/c8-7-4-2-1-3-6(7)5-9/h6-7,9H,1-5,8H2/t6-,7-/m0/s1
InChI key:InChIKey=GCWPGEWXYDEQAY-BQBZGAKWSA-N
SMILES:C(O)[C@H]1[C@@H](N)CCCC1
Synonyms:
  • (1R,2S)-2-Aminocyclohexanemethanol
  • Cyclohexanemethanol, 2-amino-, (1R,2S)-
  • ((1R,2S)-2-Aminocyclohexyl)methanol
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