(S)-2-Amino-3-cyclohexyl-propan-1-ol, with the CAS number 131288-67-0, is an organic compound characterized by its amino alcohol structure. It features a cyclohexyl group attached to a propanol backbone, which contributes to its unique physical and chemical properties. This compound is typically a chiral molecule, existing in two enantiomeric forms, with the (S) configuration being biologically relevant in various applications, particularly in pharmaceuticals. The presence of the amino group (-NH2) allows for hydrogen bonding, influencing its solubility in polar solvents, while the cyclohexyl group provides hydrophobic characteristics. This dual nature can affect its interaction with biological systems, making it a candidate for drug development. Additionally, (S)-2-Amino-3-cyclohexyl-propan-1-ol may exhibit specific biological activities, including potential roles as a neurotransmitter or in modulating receptor functions. Its synthesis and characterization are of interest in organic chemistry and medicinal chemistry, where understanding its stereochemistry is crucial for its application in therapeutic contexts.

(S)-2-Amino-3-Cyclohexyl-Propan-1-ol

131288-67-0: (S)-2-Amino-3-cyclohexyl-propan-1-ol, with the CAS number 131288-67-0, is an organic compound characterized by its amino alcohol structure. It features a cyclohexyl group attached to a propanol backbone, which contributes to its unique physical and chemical properties. This compound is typically a chiral molecule, existing in two enantiomeric forms, with the (S) configuration being biologically relevant in various applications, particularly in pharmaceuticals. The presence of the amino group (-NH2) allows for hydrogen bonding, influencing its solubility in polar solvents, while the cyclohexyl group provides hydrophobic characteristics. This dual nature can affect its interaction with biological systems, making it a candidate for drug development. Additionally, (S)-2-Amino-3-cyclohexyl-propan-1-ol may exhibit specific biological activities, including potential roles as a neurotransmitter or in modulating receptor functions. Its synthesis and characterization are of interest in organic chemistry and medicinal chemistry, where understanding its stereochemistry is crucial for its application in therapeutic contexts.

CAS 131288-67-0

(S)-2-Amino-3-Cyclohexyl-Propan-1-ol

(S)-2-Amino-3-cyclohexylpropan-1-ol

Ref: IN-DA000VUU

(S)-b-Amino-cyclohexanepropanol

Ref: 54-OR953185

(S)-b-Amino-cyclohexanepropanol

Ref: 3D-GFA28867