(S)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol is a chiral compound characterized by its specific stereochemistry, indicated by the (S) configuration at the chiral center. The presence of the Boc (tert-butyloxycarbonyl) protecting group on the amine enhances its stability and solubility, making it useful in various synthetic applications, particularly in peptide synthesis. The compound features a phenyl group, which contributes to its hydrophobic character, and a hydroxyl group that can participate in hydrogen bonding, influencing its reactivity and solubility in polar solvents. Its molecular structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals where chirality plays a crucial role in biological activity. The CAS number 718611-17-7 uniquely identifies this compound, facilitating its recognition in chemical databases and literature. Overall, (S)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol is a versatile intermediate in organic synthesis, particularly in the preparation of more complex molecules.

(S)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol

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(S)-N-Boc-3-Amino-3-phenyl-1-propanol

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CAS 718611-17-7: (S)-N-Boc-3-Amino-3-Phenyl-Propan-1-Ol

(S)-N-Boc-3-Amino-3-phenyl-1-propanol

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(S)-N-Boc-3-amino-3-phenyl-propan-1-ol

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(S)-Boc-3-Amino-3-phenylpropan-1-ol

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