1,3-Bis(Cbz-amino)-bicyclo[1.1.1]pentane is a bicyclic compound characterized by its unique structural framework, which consists of a bicyclo[1.1.1]pentane core substituted with two carbobenzoxy (Cbz) amino groups. This compound is notable for its potential applications in medicinal chemistry and peptide synthesis due to the presence of the amino groups, which can participate in various chemical reactions, including coupling reactions to form peptides. The Cbz protecting group is commonly used in organic synthesis to protect amines, allowing for selective reactions without interfering with the amino functionality. The bicyclic structure contributes to the compound's rigidity and may influence its biological activity and interaction with biological targets. Additionally, the compound's properties, such as solubility and stability, can be affected by the presence of the Cbz groups and the overall molecular conformation. As with many synthetic organic compounds, careful consideration of its reactivity and potential applications in drug development is essential for researchers working with this substance.

1,3-Bis(Cbz-aMino)-Bicyclo[1.1.1]pentane

1566649-44-2: 1,3-Bis(Cbz-amino)-bicyclo[1.1.1]pentane is a bicyclic compound characterized by its unique structural framework, which consists of a bicyclo[1.1.1]pentane core substituted with two carbobenzoxy (Cbz) amino groups. This compound is notable for its potential applications in medicinal chemistry and peptide synthesis due to the presence of the amino groups, which can participate in various chemical reactions, including coupling reactions to form peptides. The Cbz protecting group is commonly used in organic synthesis to protect amines, allowing for selective reactions without interfering with the amino functionality. The bicyclic structure contributes to the compound's rigidity and may influence its biological activity and interaction with biological targets. Additionally, the compound's properties, such as solubility and stability, can be affected by the presence of the Cbz groups and the overall molecular conformation. As with many synthetic organic compounds, careful consideration of its reactivity and potential applications in drug development is essential for researchers working with this substance.

Benzyl N-[3-(benzyloxycarbonylamino)-1-bicyclo[1.1.1]pentanyl]carbamate

<p>Dibenzyl bicyclo[1.1.1]pentane-1,3-diyldicarbamate</p>

CAS 1566649-44-2

1,3-Bis(Cbz-aMino)-Bicyclo[1.1.1]pentane

Benzyl N-[3-(benzyloxycarbonylamino)-1-bicyclo[1.1.1]pentanyl]carbamate

Ref: IN-DA001OVP

Dibenzyl bicyclo[1.1.1]pentane-1,3-diyldicarbamate

Ref: 54-OR312454