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Catalog Number:
41563
CAS Number:
168049-26-1
( S )-2-(azidométhyl)-1-Boc-pyrrolidine
Purity:
≥ 98 % (pureté chirale)
Synonym(s):
( S )-2-(azidométhyl)-1-( tert -butoxycarbonyl)pyrrolidine, tert -butyl( S )-2-(azidométhyl)-1-pyrrolidinecarboxylate
Documents
$54.08 /100 mg
Taille
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Informations sur le produit

(S)-2-(Azidomethyl)-1-Boc-pyrrolidine is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a tert-butyl protective group, which enhances its stability and reactivity, making it an excellent choice for researchers looking to develop new pharmaceuticals or advanced materials. Its unique azidomethyl functionality allows for further modifications, facilitating the introduction of various functional groups through click chemistry, which is particularly valuable in drug discovery and development.

In addition to its applications in synthetic organic chemistry, (S)-2-(Azidomethyl)-1-Boc-pyrrolidine is also employed in the preparation of complex molecules, including potential therapeutics and biologically active compounds. Its ability to serve as a building block in the synthesis of more intricate structures underscores its importance in both academic research and industrial applications. Researchers and professionals can leverage this compound to streamline their synthesis processes while achieving high yields and purity.

Numéro CAS 
168049-26-1
Formule moléculaire
C10H18N4O2
Poids moléculaire 
226.28
Rotation optique 
[ á]/D = -48,5 ± 1 ° (C = 1 dans le chloroforme)
Informations générales
Numéro CAS 
168049-26-1
Formule moléculaire
C10H18N4O2
Poids moléculaire 
226.28
Rotation optique 
[ á]/D = -48,5 ± 1 ° (C = 1 dans le chloroforme)
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)-2-(Azidomethyl)-1-Boc-pyrrolidine is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique azido group allows for click chemistry applications, facilitating the creation of complex drug candidates with improved efficacy and specificity.
  • Bioconjugation: The azide functionality enables bioconjugation techniques, which are essential in creating targeted therapies and diagnostic agents in the biomedical field.
  • Material Science: It can be used in the development of functionalized polymers and materials, enhancing properties such as biocompatibility and mechanical strength.
  • Research and Development: This compound is valuable in academic and industrial research settings for exploring new reaction pathways and mechanisms, aiding in the advancement of chemical knowledge.

Citations