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Catalog Number:
29684
CAS Number:
203854-62-0
Acide S -Fmoc-3-amino-2-benzyl-propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S -Fmoc-β2-homophénylalanine
Documents
$127.79 /25 mg
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Product Information

(S)-Fmoc-3-amino-2-benzyl-propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focused on developing complex peptide sequences. The presence of the benzyl group enhances its stability and solubility, facilitating easier handling and incorporation into various chemical reactions.

In addition to its role in peptide synthesis, (S)-Fmoc-3-amino-2-benzyl-propionic acid is also valuable in the pharmaceutical industry for the development of bioactive compounds. Its ability to provide a stable and easily removable protecting group allows chemists to streamline the synthesis process, ultimately leading to more efficient production of therapeutic peptides. Researchers in medicinal chemistry and biochemistry will find this compound particularly beneficial for its practicality and effectiveness in producing high-purity peptides with desired biological activities.

Synonyms
( S -Fmoc-β2-homophénylalanine
CAS Number
203854-62-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 234
Molecular Weight
401.46
MDL Number
MFCD07372497
PubChem ID
44118845
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = -6,0 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
( S -Fmoc-β2-homophénylalanine
CAS Number
203854-62-0
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 234
Molecular Weight
401.46
MDL Number
MFCD07372497
PubChem ID
44118845
Appearance
Poudre blanche
Optical Rotation
[α] D 20 = -6,0 ± 2º (C = 1 dans DMF)
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

(S)-Fmoc-3-amino-2-benzyl-propionic 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), where its Fmoc (fluorenylmethyloxycarbonyl) protection group allows for selective deprotection and coupling reactions.
  • Drug Development: Its structural properties make it valuable in the design of pharmaceutical compounds, particularly in developing drugs that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules such as proteins and antibodies to therapeutic agents, improving targeted delivery and therapeutic outcomes.
  • Research in Neuroscience: It is applied in the study of neuropeptides, contributing to research on neurological disorders and potential treatments by facilitating the synthesis of neuroactive peptides.
  • Custom Peptide Libraries: Researchers utilize this compound to create diverse peptide libraries for screening in drug discovery, allowing for the identification of novel compounds with desired biological activities.

Citations