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Catalog Number:
16743
CAS Number:
151215-34-8
Acide boc-L-2-amino-4-bromo-4-penténoïque
Purity:
≥ 99 % (HPLC, pureté chirale)
Synonym(s):
Boc-( S -(2-bromoallyl)glycine
Documents
$65.40 /100 mg
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Product Information

Boc-L-2-amino-4-bromo-4-pentenoic acid is a versatile building block in peptide synthesis and medicinal chemistry. This compound features a bromo substituent that enhances its reactivity, making it an ideal candidate for the development of novel peptides and bioactive molecules. Its unique structure allows for the introduction of various functional groups, facilitating the design of compounds with specific biological activities. Researchers in the pharmaceutical industry can leverage this compound to create targeted therapies, particularly in the fields of oncology and neurobiology, where precise molecular interactions are crucial.

Additionally, Boc-L-2-amino-4-bromo-4-pentenoic acid serves as an important intermediate in the synthesis of amino acid derivatives and can be utilized in the preparation of peptide libraries for drug discovery. Its stability and ease of handling make it a preferred choice for both academic and industrial applications. With its potential to enhance the efficacy of therapeutic agents, this compound is a valuable asset for professionals seeking innovative solutions in drug development.

Synonyms
Boc-( S -(2-bromoallyl)glycine
CAS Number
151215-34-8
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C10H16BrNO4
Molecular Weight
294.14
MDL Number
MFCD01320852
PubChem ID
53398429
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 25 = -7 ± 0,5º (C = 1 dans EtOH)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-( S -(2-bromoallyl)glycine
CAS Number
151215-34-8
Purity
≥ 99 % (HPLC, pureté chirale)
Molecular Formula
C10H16BrNO4
Molecular Weight
294.14
MDL Number
MFCD01320852
PubChem ID
53398429
Appearance
Poudre cristalline blanche
Optical Rotation
[a] D 25 = -7 ± 0,5º (C = 1 dans EtOH)
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Boc-L-2-amino-4-bromo-4-pentenoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of novel therapeutic agents.
  • Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their efficacy and selectivity in targeting specific biological pathways.
  • Bioconjugation: The compound can be used in bioconjugation processes to attach biomolecules to surfaces or other molecules, facilitating the creation of targeted drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, particularly in the development of compounds that can modulate synaptic transmission.
  • Material Science: The compound is explored for its potential applications in creating advanced materials with specific properties, such as improved thermal stability and mechanical strength.

Citations