🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
14843
CAS Number:
1448613-98-6
Nα-Fmoc-Nβ-bromoacetyl-L-2,3-diaminopropionic acid
Purity:
≥ 95% (HPLC)
Synonym(s):
Fmoc-L-Dap(bromoacetyl)-OH, 2-Fmoc-amino-3-(2-bromoacetamido)propanoic acid
Documents
$150.00 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Na-Fmoc-Nb-bromoacetyl-L-2,3-diaminopropionic acid is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a bromoacetyl group that enhances its reactivity, making it an excellent building block for the creation of complex peptides and bioactive molecules. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating the synthesis of peptides with high purity and yield. Researchers in medicinal chemistry and biochemistry can leverage this compound for the development of targeted therapeutics, particularly in the design of peptide-based drugs that require precise structural modifications.

In addition to its applications in peptide synthesis, Na-Fmoc-Nb-bromoacetyl-L-2,3-diaminopropionic acid can also be employed in the study of protein interactions and enzyme activity. Its unique structure allows for the incorporation of specific functionalities that can be tailored to enhance binding affinity or specificity in biological assays. This compound stands out due to its dual functionality, making it a valuable asset for researchers aiming to explore new avenues in drug discovery and development.

Synonyms
Fmoc-L-Dap(bromoacetyl)-OH, 2-Fmoc-amino-3-(2-bromoacetamido)propanoic acid
CAS Number
1448613-98-6
Purity
≥ 95% (HPLC)
Molecular Formula
C20H19BrN2O5
Molecular Weight
447.29
MDL Number
MFCD08458575
PubChem ID
139211112
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-L-Dap(bromoacetyl)-OH, 2-Fmoc-amino-3-(2-bromoacetamido)propanoic acid
CAS Number
1448613-98-6
Purity
≥ 95% (HPLC)
Molecular Formula
C20H19BrN2O5
Molecular Weight
447.29
MDL Number
MFCD08458575
PubChem ID
139211112
Appearance
White to off-white powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Fmoc-Nb-bromoacetyl-L-2,3-diaminopropionic 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, allowing for the creation of complex peptide chains with high purity.
  • Drug Development: It plays a significant role in the development of novel pharmaceuticals, especially in creating peptide-based drugs that can target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The bromoacetyl group enables efficient bioconjugation, making it ideal for attaching peptides to various biomolecules, which is crucial in creating targeted drug delivery systems.
  • Research in Neuroscience: It is used in studies related to neuropeptides, helping researchers understand the role of specific peptides in neurological functions and disorders.
  • Custom Synthesis: This compound is valuable for researchers needing tailored peptide sequences for specific applications, providing flexibility in designing experiments and therapeutic agents.

Citations