235788-61-1

Basic information

• Product Name: FMOC-L-DAB(DDE)-OH
• Synonyms: (S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-4-((1-(4,4-diMethyl-2,6-dioxocyclohexylidene)ethyl)aMino)butanoic acid;Fmoc-Dab(Dde);Fmoc-(N-gamma-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-alpha,gamma-diaminobutyric;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-GAMMA-(4,4-DIMETHYL-2,6-DIOXOCYCLOHEX-1-YLIDENE)ETHYL-L-2,4-DIAMINOBUTYRIC ACID;FMOC-L-DAB(DDE)-OH;(2S)-4-[[1-(4,4-Dimethyl-2,6-dioxocyclohexylidene)ethyl]amino]-2-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]butanoic acid;Fmoc-(N-gamma-1-(4,4-dimethyl-2,6-dioxocyclohex-1-ylidene)ethyl)-L-alpha,gamma-diaminobutyric aci;(9H-Fluoren-9-yl)MethOxy]Carbonyl Dab(Dde)-OH
• CAS NO: 235788-61-1
• Molecular Formula: C29H32N2O6
• Molecular Weight: 504.57
• Product Categories: amino acids
• Mol File: 235788-61-1.mol

Chemical Properties

• Boiling Point: 736.3±60.0 °C(Predicted)
• Appearance: /
• Density: 1.252
• Storage Temp.: 2-8°C
• PKA: 3.74±0.10(Predicted)
• CAS DataBase Reference: FMOC-L-DAB(DDE)-OH(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-L-DAB(DDE)-OH(235788-61-1)
• EPA Substance Registry System: FMOC-L-DAB(DDE)-OH(235788-61-1)

Safety Data

• Hazardous Substances Data: 235788-61-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
FMOC-L-DAB(DDE)-OH is used as a key intermediate in the synthesis of peptide-based drugs for various therapeutic applications. Its chiral center and protecting group enable the creation of peptide analogs with specific biological activities, such as modulating immune responses, targeting cancer cells, or treating neurological disorders.
Used in Chemical Research:
FMOC-L-DAB(DDE)-OH is employed as a building block in the development of novel chemical compounds with potential applications in various fields, including materials science, catalysis, and environmental remediation. Its unique structure allows for the exploration of new chemical reactions and the synthesis of innovative molecules with tailored properties.
Used in Biological Research:
FMOC-L-DAB(DDE)-OH is utilized as a component in the synthesis of peptide probes for studying protein-protein interactions, enzyme substrate specificity, and other biological processes. Its chiral center and protecting group facilitate the design of peptide-based tools that can selectively target and modulate specific biological systems, providing valuable insights into cellular mechanisms and potential therapeutic targets.
Used in Peptide Synthesis Education:
FMOC-L-DAB(DDE)-OH serves as an educational tool in teaching the principles and techniques of solid-phase peptide synthesis. Its structure and reactivity provide a practical example for students to understand the importance of protecting groups, chirality, and the stepwise assembly of peptide chains in modern peptide synthesis methods.