946682-26-4

Basic information

• Product Name: (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected
• Synonyms: (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected;2-(4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)piperidin-4-yl)acetic acid;2-(4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-1-(tert-butoxycarbonyl)piperidin-4-yl)acetic acid(WXC06693)
• CAS NO: 946682-26-4
• Molecular Formula: C7H14N2O2
• Molecular Weight: 158.19826
• Mol File: 946682-26-4.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected(CAS DataBase Reference)
• NIST Chemistry Reference: (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected(946682-26-4)
• EPA Substance Registry System: (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected(946682-26-4)

Safety Data

• Hazardous Substances Data: 946682-26-4(Hazardous Substances Data)

Usage

Description

(4-Aminopiperidin-4-yl)acetic acid, N1-BOC4-FMOCprotected is a chemical compound belonging to the class of amino acids. It is a derivative of piperidine, a heterocyclic compound with a six-membered ring containing one nitrogen atom. (4-Aminopiperidin-4-yl)aceticacid,N1-BOC4-FMOCprotected features N-protection with both BOC and FMOC groups, which are widely used to protect amine groups during peptide synthesis. The presence of these protective groups makes it suitable for applications in peptide chemistry, including the synthesis of peptide libraries and combinatorial chemistry.

Uses

Used in Pharmaceutical Industry:
(4-Aminopiperidin-4-yl)acetic acid, N1-BOC4-FMOCprotected is used as a building block for the development of peptide-based drugs and drug discovery research. Its unique structure and N-protection with BOC and FMOC groups make it a valuable component in the synthesis of novel therapeutic agents.
Used in Peptide Synthesis:
In the field of peptide chemistry, (4-Aminopiperidin-4-yl)acetic acid, N1-BOC4-FMOCprotected is used as a protected amino acid for the synthesis of complex peptide sequences. The BOC and FMOC groups protect the amine group during the coupling reactions, preventing unwanted side reactions and ensuring the formation of the desired peptide product.
Used in Combinatorial Chemistry:
(4-Aminopiperidin-4-yl)acetic acid, N1-BOC4-FMOCprotected is also utilized in combinatorial chemistry for the generation of diverse peptide libraries. These libraries are essential for high-throughput screening and the identification of potential drug candidates with specific biological activities.