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Catalog Number:
05604
CAS Number:
71404-98-3
Boc-β-chloro-L-alanine
Purity:
≥ 95 % (RMN)
Synonym(s):
Boc-β-chloro-L-Ala-OH, Boc-3-Chloro-L-alanine
Documents
$127.79 /1G
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Product Information

Boc-b-chloro-L-alanine is a versatile amino acid derivative that plays a significant role in peptide synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers focused on developing novel peptides and pharmaceuticals. Its unique chloro substituent allows for selective reactions, facilitating the incorporation of this amino acid into more complex structures.

In practical applications, Boc-b-chloro-L-alanine is utilized in the synthesis of bioactive peptides, which can be pivotal in drug discovery and development. Its ability to undergo various coupling reactions makes it a valuable building block in the creation of peptide libraries for screening potential therapeutic agents. Additionally, its stability under various reaction conditions ensures consistent results, making it a preferred choice among researchers and industry professionals alike. With its robust properties and wide-ranging applications, Boc-b-chloro-L-alanine stands out as a key compound for advancing peptide chemistry and pharmaceutical research.

Synonyms
Boc-β-chloro-L-Ala-OH, Boc-3-Chloro-L-alanine
CAS Number
71404-98-3
Purity
≥ 95 % (RMN)
Molecular Formula
C8H14NO4Cl
Molecular Weight
223.66
MDL Number
MFCD00672318
PubChem ID
21778988
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -4,0 ± 2º (C = 1 % dans CHCl 3 )
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Boc-β-chloro-L-Ala-OH, Boc-3-Chloro-L-alanine
CAS Number
71404-98-3
Purity
≥ 95 % (RMN)
Molecular Formula
C8H14NO4Cl
Molecular Weight
223.66
MDL Number
MFCD00672318
PubChem ID
21778988
Appearance
Poudre blanche à blanc cassé
Optical Rotation
[a] D 25 = -4,0 ± 2º (C = 1 % dans CHCl 3 )
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-b-chloro-L-alanine is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in the development of inhibitors and other bioactive compounds that target specific biological pathways.
  • Bioconjugation: The unique properties of Boc-b-chloro-L-alanine facilitate its use in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds for targeted delivery systems.
  • Research in Neuroscience: This compound is employed in studies related to neurotransmitter activity, helping scientists understand the mechanisms of action for various neurological disorders.
  • Protein Engineering: It is utilized in protein engineering applications, allowing for the modification of proteins to enhance their stability and activity, which is essential in biotechnological applications.

Citations