Product Name:Tert-Butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate

IUPAC Name:tert-butyl N-{4-aminobicyclo[2.2.2]octan-1-yl}carbamate

CAS:1630906-54-5
Molecular Formula:C13H24N2O2
Purity:95%
Catalog Number:CM294152
Molecular Weight:240.35

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Product Details

CAS NO:1630906-54-5
Molecular Formula:C13H24N2O2
Melting Point:-
Smiles Code:O=C(OC(C)(C)C)NC1(CC2)CCC2(N)CC1
Density:
Catalog Number:CM294152
Molecular Weight:240.35
Boiling Point:342.5±41.0°C at 760 mmHg
MDL No:
Storage:Keep in dark place, store at 2-8°C.

Category Infos

Bridged Compounds
Bridged ring compound refers to any two rings in the compound, which share two non-directly connected carbon atoms, and are classified into bicyclic hydrocarbons, tricyclic hydrocarbons, tetracyclic hydrocarbons, etc. Carbon atoms used in two or more rings are bridgehead carbon atoms, and the bond connecting the bridgehead carbon atoms is called a bridge. Bridged ring compounds are a class of organic compounds that are widely present in nature and usually have important physiological activities, such as the famous anticancer drug paclitaxel and antimalarial drug artemisinin.
bridged compounds,bridged bicyclic compounds
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Product Other Information

Product Overview Tert-Butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate, also known as t-Boc-Aminocyclopentane, is a versatile and widely used carbamate in various fields of science. It is a commonly used reagent in organic synthesis and has many applications in the fields of biochemistry, pharmaceuticals, and materials science.
Physical Properties It is a white crystalline solid that is soluble in common organic solvents such as methanol, ethanol, and acetone.
Synthesis and Application Tert-butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate can be synthesized by reacting tert-butyl isocyanate with 4-aminocyclopentane in the presence of a base. The reaction is typically carried out in an organic solvent such as dichloromethane or toluene at temperatures ranging from 0 to 50°C. The reaction is complete when the reaction mixture is neutralized with an acid such as hydrochloric acid. Tert-butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate has a variety of scientific research applications. It is commonly used as a protecting group for amines in peptide synthesis, as a reagent in the synthesis of peptides, as a catalyst for the preparation of cyclic carbonates, and as a reagent in the synthesis of heterocyclic compounds. Additionally, it has been used in the development of peptide-based drugs, the synthesis of peptide-based vaccines, and the synthesis of peptide-based contrast agents for magnetic resonance imaging (MRI).
Future Directions The future of tert-butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate is promising. It is a versatile reagent with a variety of applications in organic synthesis. It can be used to synthesize peptides, cyclic carbonates, and heterocyclic compounds. Additionally, it can be used in the development of peptide-based drugs, peptide-based vaccines, and peptide-based contrast agents for MRI. Furthermore, research is ongoing to develop new methods for the synthesis of peptides using tert-butyl carbamate. Finally, new derivatives of tert-butyl carbamate are being developed for use as protecting groups in peptide synthesis.