117106-22-6

Basic information

• Product Name: (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid
• CAS NO: 117106-22-6
• Molecular Weight: 340.379
• Mol File: 117106-22-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid(117106-22-6)
• EPA Substance Registry System: (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid(117106-22-6)

Safety Data

• Hazardous Substances Data: 117106-22-6(Hazardous Substances Data)

Usage

General Description

(S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid is a chemical compound with a complex structure. It contains a fluorene group, a carbonyl group, an amino group, and a butanoic acid group. (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid is a chiral molecule, as indicated by the (S) in its name, meaning it has a non-superposable mirror image. It may have potential applications in pharmaceuticals, materials science, or other fields due to its unique structure and properties. However, further research and development would be needed to determine its specific uses and potential benefits.

Upstream product

• 117106-21-5 N^α-t-Boc-N^γ-(9-fluorenylmethyloxycarbonyl)-(L)-2,4-diaminobutyric acid 
• 82911-69-1 N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide 
• 1482-98-0 (S)-2,4-diaminobutyric acid dihydrochloride 

Downstream Products

• 117106-21-5 N^α-t-Boc-N^γ-(9-fluorenylmethyloxycarbonyl)-(L)-2,4-diaminobutyric acid 
• 1072896-05-9 N^γ-Fmoc-N^α-[N⁶-(benzhydryloxycarbonyl)-(adenin-9-yl)acetyl]-2,4-diaminobutyric acid 

Relevant articles and documents

dabPNA: Design, synthesis, and DNA binding studies

In continuing our research efforts for developing new oligodeoxynucleotide (ODN)-like drugs and diagnostics, we designed diaminobutyric peptide nucleic acids (dabPNAs), nucleopeptides characterized by a diaminobutyric-based building block that is an isomer of the aminoethylglycyl PNA (aegPNA) unit and the acyclic modification of the aminoprolyl PNA (ampPNA) monomer. In this work we present the solid phase synthesis of a dabPNA oligomer and of two aegPNAs containing a single dabPNA unit. A study relative to their binding ability towards DNA is also reported even in comparison with the well known aegPNAs. Copyright Taylor & Francis Group, LLC.

Synthesis of linear undecapeptide precursors of cyclosporin analogues

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