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Catalog Number:
41472
CAS Number:
839710-38-2
Acide ( S )-4-Boc-3-morpholinacétique
Purity:
≥ 97 % (pureté chirale)
Synonym(s):
( S )- N -Boc-3-carboxyméthyl-morpholine, Acide ( S )-1-Boc-morpholin-3-ylacétique
Documents
$213.62 /250 mg
Taille
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Informations sur le produit

(S)-4-Boc-3-morpholineacetic acid is a versatile compound widely utilized in pharmaceutical and chemical research. This chiral building block is particularly valuable in the synthesis of various bioactive molecules, including potential drug candidates. Its unique morpholine structure enhances solubility and bioavailability, making it an ideal choice for medicinal chemistry applications. Researchers appreciate its ability to facilitate the development of compounds with improved pharmacological profiles, particularly in the areas of analgesics and anti-inflammatory agents.

Additionally, (S)-4-Boc-3-morpholineacetic acid serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. This characteristic is crucial for chemists aiming to create complex peptide structures with high specificity. Its stability under various reaction conditions further underscores its utility in synthetic pathways, providing researchers with a reliable tool for advancing their projects. With its broad range of applications, this compound is essential for those looking to innovate in drug discovery and development.

Numéro CAS 
839710-38-2
Formule moléculaire
C 11 H 195
Poids moléculaire 
245.27
Rotation optique 
[ á]/D = 36 ° (C = 2 dans le chlorure de méthylène)
Informations générales
Numéro CAS 
839710-38-2
Formule moléculaire
C 11 H 195
Poids moléculaire 
245.27
Rotation optique 
[ á]/D = 36 ° (C = 2 dans le chlorure de méthylène)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

(S)-4-Boc-3-morpholineacetic acid is widely utilized in research focused on

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting neurological disorders. Its unique structure enhances drug efficacy and bioavailability.
  • Peptide Synthesis: It is commonly used in the formation of peptide bonds, facilitating the creation of complex peptides that are crucial for therapeutic applications and research in biochemistry.
  • Drug Delivery Systems: The compound can be incorporated into drug delivery formulations, improving the stability and release profiles of active pharmaceutical ingredients, which is essential for effective treatment regimens.
  • Bioconjugation: Its reactive functional groups allow for bioconjugation processes, enabling the attachment of drugs or imaging agents to biomolecules, which is vital in targeted therapy and diagnostic applications.
  • Research in Chemical Biology: This chemical is instrumental in chemical biology studies, helping researchers understand enzyme mechanisms and protein interactions, thereby advancing knowledge in cellular processes.

Citations