The chemical substance with the name "(2S,4S,5S,7S)-N-(3-amino-2,2-dimethyl-3-oxopropyl)-5-azido-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide" and CAS number "324763-47-5" is a complex organic compound characterized by multiple functional groups and stereocenters. It features an azido group, which is notable for its reactivity and potential applications in click chemistry. The presence of hydroxy and amine groups suggests it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The isopropyl and methoxy substituents contribute to its hydrophobic characteristics, while the nonanamide backbone indicates a relatively long carbon chain, which may affect its biological activity and membrane permeability. The stereochemistry, indicated by the (2S,4S,5S,7S) configuration, suggests specific spatial arrangements that could be critical for its interaction with biological targets. Overall, this compound's unique structure may lend itself to applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a biochemical probe.

(2S,4S,5S,7S)-N-(3-amino-2,2-dimethyl-3-oxopropyl)-5-azido-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

324763-47-5: The chemical substance with the name "(2S,4S,5S,7S)-N-(3-amino-2,2-dimethyl-3-oxopropyl)-5-azido-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide" and CAS number "324763-47-5" is a complex organic compound characterized by multiple functional groups and stereocenters. It features an azido group, which is notable for its reactivity and potential applications in click chemistry. The presence of hydroxy and amine groups suggests it may exhibit hydrogen bonding capabilities, influencing its solubility and reactivity. The isopropyl and methoxy substituents contribute to its hydrophobic characteristics, while the nonanamide backbone indicates a relatively long carbon chain, which may affect its biological activity and membrane permeability. The stereochemistry, indicated by the (2S,4S,5S,7S) configuration, suggests specific spatial arrangements that could be critical for its interaction with biological targets. Overall, this compound's unique structure may lend itself to applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a biochemical probe.

<p>Applications Intermediate in the preparation of renin inhibitors.<br>References Sandham, D. et al.: Tetrahedron Lett., 41, 10091 (2000)<br></p>

CAS 324763-47-5

(2S,4S,5S,7S)-N-(3-amino-2,2-dimethyl-3-oxopropyl)-5-azido-4-hydroxy-2-isopropyl-7-(4-methoxy-3-(3-methoxypropoxy)benzyl)-8-methylnonanamide

5-Azido-5-desamino Aliskiren-d6

Ref: TR-A827362