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

Description

(S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid is a complex chemical compound characterized by its fluorene, carbonyl, amino, and butanoic acid groups. As a chiral molecule, it possesses a non-superposable mirror image, denoted by the (S) in its name. This unique structure and properties suggest potential applications in various fields, such as pharmaceuticals and materials science, although further research and development are required to ascertain its specific uses and benefits.

Uses

Used in Pharmaceutical Industry:
(S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid is used as a potential pharmaceutical compound for its unique structure and properties, which may contribute to the development of new drugs or therapies.
Used in Materials Science:
(S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminobutanoic acid is used as a potential material in materials science due to its complex structure, which may offer novel properties for the development of advanced materials.

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

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