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Catalog Number:
06302
CAS Number:
135630-90-9
Ácido N α - Boc- N β -bromoacetil-L-2,3-diaminopropiónico
Purity:
≥ 98%
Synonym(s):
Boc-L-Dap(bromoacetil)-OH
Documents
$255.48 /1G
Tamaño
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Product Information

Na-Boc-Nb-bromoacetyl-L-2,3-diaminopropionic acid is a versatile compound that plays a significant role in peptide synthesis and drug development. This amino acid derivative features a bromoacetyl group, which enhances its reactivity, making it an excellent candidate for various chemical modifications. Its unique structure allows for the introduction of diverse functional groups, facilitating the design of novel bioactive molecules. Researchers in medicinal chemistry and biochemistry can leverage this compound for the development of targeted therapeutics, particularly in the fields of cancer treatment and antimicrobial agents.

Additionally, Na-Boc-Nb-bromoacetyl-L-2,3-diaminopropionic acid is recognized for its stability and ease of handling, which are critical for laboratory applications. Its ability to form stable conjugates with other biomolecules opens avenues for creating advanced drug delivery systems. This compound stands out due to its specific reactivity profile compared to similar amino acid derivatives, making it a valuable tool for scientists aiming to innovate in drug design and synthesis.

Synonyms
Boc-L-Dap(bromoacetil)-OH
CAS Number
135630-90-9
Purity
≥ 98%
Molecular Formula
C10H17N2O5Br
Molecular Weight
325.2
MDL Number
MFCD00798614
PubChem ID
78439113
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Dap(bromoacetil)-OH
CAS Number
135630-90-9
Purity
≥ 98%
Molecular Formula
C10H17N2O5Br
Molecular Weight
325.2
MDL Number
MFCD00798614
PubChem ID
78439113
Appearance
Polvo blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na-Boc-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, enabling the incorporation of specific functional groups that enhance biological activity.
  • Drug Development: It plays a crucial role in the development of novel pharmaceuticals, particularly in designing compounds that target specific proteins or enzymes in disease pathways.
  • Bioconjugation: The bromoacetyl group allows for selective conjugation with biomolecules, facilitating the creation of targeted drug delivery systems and improving therapeutic efficacy.
  • Research in Biochemistry: It is used in various biochemical assays to study enzyme interactions and protein folding, providing insights into cellular processes.
  • Material Science: The compound can be employed in the development of smart materials that respond to environmental stimuli, showcasing its versatility beyond traditional applications.

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