3-(Boc-amino)-3-(3-chlorophenyl)-1-propanol is a chemical compound characterized by its structural features, which include a tert-butoxycarbonyl (Boc) protecting group attached to an amino group, a chlorophenyl moiety, and a propanol backbone. The presence of the Boc group indicates that the amino group is protected, making it suitable for various synthetic applications, particularly in peptide synthesis and medicinal chemistry. The 3-chlorophenyl group contributes to the compound's hydrophobic characteristics and may influence its biological activity. The propanol portion of the molecule provides a chiral center, which can lead to enantiomeric forms with potentially different properties. This compound is typically used in research and development, particularly in the synthesis of pharmaceuticals or biologically active molecules. Its specific reactivity and interactions would depend on the functional groups present and the overall molecular structure, making it a versatile intermediate in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with its components.

3-(Boc-aMino)-3-(3-chlorophenyl)-1-propanol

1314406-54-6: 3-(Boc-amino)-3-(3-chlorophenyl)-1-propanol is a chemical compound characterized by its structural features, which include a tert-butoxycarbonyl (Boc) protecting group attached to an amino group, a chlorophenyl moiety, and a propanol backbone. The presence of the Boc group indicates that the amino group is protected, making it suitable for various synthetic applications, particularly in peptide synthesis and medicinal chemistry. The 3-chlorophenyl group contributes to the compound's hydrophobic characteristics and may influence its biological activity. The propanol portion of the molecule provides a chiral center, which can lead to enantiomeric forms with potentially different properties. This compound is typically used in research and development, particularly in the synthesis of pharmaceuticals or biologically active molecules. Its specific reactivity and interactions would depend on the functional groups present and the overall molecular structure, making it a versatile intermediate in organic synthesis. Safety and handling precautions should be observed, as with all chemical substances, due to potential hazards associated with its components.

tert-Butyl (1-(3-chlorophenyl)-3-hydroxypropyl)carbamate

3-(Boc-amino)-3-(3-chlorophenyl)-1-propanol

CAS 1314406-54-6

3-(Boc-aMino)-3-(3-chlorophenyl)-1-propanol

tert-Butyl (1-(3-chlorophenyl)-3-hydroxypropyl)carbamate

Ref: IN-DA000W6Z

3-(Boc-amino)-3-(3-chlorophenyl)-1-propanol

Ref: 54-OR470354