Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
16744
CAS Number:
220497-92-7
Fmoc-D-2-amino-4-bromo-4-pentenoic acid
Purity:
≥ 99% (Chiral HPLC, HPLC)
Synonym(s):
Fmoc-(R)-(2-bromoallyl)glycine
Documents
$80.50 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-D-2-amino-4-bromo-4-pentenoic acid is a specialized amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which allows for selective deprotection during the synthesis process, making it an invaluable tool for researchers in the field of organic chemistry. Its bromo and pentenoic acid functionalities enhance its reactivity, enabling the formation of complex peptide structures that are essential in drug development and biological research.

This compound is particularly beneficial in the synthesis of bioactive peptides, which can be used in therapeutic applications, including cancer treatment and antibiotic development. Its ability to facilitate the introduction of specific functional groups into peptides provides researchers with the flexibility needed to design novel compounds with enhanced biological activity. With its robust properties and versatility, Fmoc-D-2-amino-4-bromo-4-pentenoic acid stands out as a key reagent for professionals aiming to innovate in peptide-based therapies.

Synonyms
Fmoc-(R)-(2-bromoallyl)glycine
CAS Number
220497-92-7
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C20H18BrNO4
Molecular Weight
416.27
MDL Number
MFCD01311777
PubChem ID
53397922
Appearance
White powder or yellowish solid
Optical Rotation
[a]D25 = 10 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-(R)-(2-bromoallyl)glycine
CAS Number
220497-92-7
Purity
≥ 99% (Chiral HPLC, HPLC)
Molecular Formula
C20H18BrNO4
Molecular Weight
416.27
MDL Number
MFCD01311777
PubChem ID
53397922
Appearance
White powder or yellowish solid
Optical Rotation
[a]D25 = 10 ± 2 º (C=1 in MeOH)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-D-2-amino-4-bromo-4-pentenoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS), allowing for the creation of complex peptide sequences with high purity.
  • Drug Development: Its unique structure makes it valuable in medicinal chemistry for the design of novel therapeutic agents, especially in targeting specific biological pathways.
  • Bioconjugation: This chemical can be used to create bioconjugates, linking biomolecules to drugs or imaging agents, enhancing the efficacy and targeting of treatments in areas like cancer therapy.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, helping researchers understand the role of specific amino acids in neurobiology.
  • Material Science: The compound can be incorporated into polymers to develop materials with specific properties, such as improved biocompatibility for medical devices.

Citations