1330763-51-3

Basic information

• Product Name: 8-AMino-3-Boc-3-azabicyclo[3.2.1]octane
• Synonyms: 8-AMino-3-Boc-3-azabicyclo[3.2.1]octane;8-Amino-3-aza-bicyclo[3.2.1]octane-3-carboxylic acid tert-butyl ester;tert-Butyl 8-amino-3-azabicyclo[3.2.1]octane-3-carboxylate
• CAS NO: 1330763-51-3
• Molecular Formula: C12H22N2O2
• Molecular Weight: 226.31528
• Mol File: 1330763-51-3.mol

Chemical Properties

• Boiling Point: 313.2±35.0 °C(Predicted)
• Appearance: /
• Density: 1.084±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C(protect from light)
• PKA: 10.01±0.20(Predicted)
• CAS DataBase Reference: 8-AMino-3-Boc-3-azabicyclo[3.2.1]octane(CAS DataBase Reference)
• NIST Chemistry Reference: 8-AMino-3-Boc-3-azabicyclo[3.2.1]octane(1330763-51-3)
• EPA Substance Registry System: 8-AMino-3-Boc-3-azabicyclo[3.2.1]octane(1330763-51-3)

Safety Data

• Hazardous Substances Data: 1330763-51-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Development:
8-Amino-3-Boc-3-azabicyclo[3.2.1]octane is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new drugs. Its unique aza-bridged bicyclic structure allows for the creation of diverse molecular architectures with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 8-Amino-3-Boc-3-azabicyclo[3.2.1]octane serves as a valuable precursor to a range of chemical compounds. Its Boc-protected amino group facilitates selective reactions, enabling chemists to construct complex molecules with precision and control.
Used in Protecting Group Chemistry:
8-Amino-3-Boc-3-azabicyclo[3.2.1]octane is utilized as a protecting group for the amino functionality in organic synthesis. The Boc group temporarily masks the amino group, allowing for selective reactions to occur at other sites within the molecule. This selective protection is crucial for the synthesis of complex organic compounds and the development of advanced pharmaceutical agents.