2-(3-BOC-Aminophenyl)phenol, identified by its CAS number 1261900-37-1, is an organic compound characterized by the presence of a phenolic group and a tert-butyloxycarbonyl (BOC) protecting group attached to an amino group. This compound typically exhibits properties associated with both phenols and amines, such as moderate solubility in organic solvents and potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions. The BOC group serves as a protective moiety for the amino functionality, allowing for selective reactions without interfering with the amine's reactivity. In terms of applications, compounds like this are often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The presence of both the phenolic and amino functionalities can also contribute to hydrogen bonding and other intermolecular interactions, influencing the compound's physical properties and behavior in different environments. Overall, 2-(3-BOC-Aminophenyl)phenol is a versatile building block in synthetic organic chemistry.

2-(3-BOC-AMinophenyl)phenol

1261900-37-1: 2-(3-BOC-Aminophenyl)phenol, identified by its CAS number 1261900-37-1, is an organic compound characterized by the presence of a phenolic group and a tert-butyloxycarbonyl (BOC) protecting group attached to an amino group. This compound typically exhibits properties associated with both phenols and amines, such as moderate solubility in organic solvents and potential reactivity in various chemical reactions, including nucleophilic substitutions and coupling reactions. The BOC group serves as a protective moiety for the amino functionality, allowing for selective reactions without interfering with the amine's reactivity. In terms of applications, compounds like this are often utilized in medicinal chemistry and organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. The presence of both the phenolic and amino functionalities can also contribute to hydrogen bonding and other intermolecular interactions, influencing the compound's physical properties and behavior in different environments. Overall, 2-(3-BOC-Aminophenyl)phenol is a versatile building block in synthetic organic chemistry.

CAS 1261900-37-1

2-(3-BOC-AMinophenyl)phenol

2-(3-BOC-Aminophenyl)phenol

Ref: IN-DA000S4K