CAS 333366-32-8
:(S)-(−)-2-Azido-6-(Boc-amino)hexanoic acid
Description:
(S)-(−)-2-Azido-6-(Boc-amino)hexanoic acid is a chiral compound characterized by the presence of an azido group and a Boc (tert-butyloxycarbonyl) protecting group on the amino functional group. This compound features a hexanoic acid backbone, which contributes to its aliphatic nature. The azido group (-N3) is known for its reactivity, particularly in click chemistry applications, making this compound valuable in synthetic organic chemistry and bioconjugation. The Boc group serves as a protective moiety for the amino group, allowing for selective reactions without interfering with the amine functionality. The stereochemistry indicated by the (S) configuration suggests that the compound exhibits specific optical activity, which is crucial in applications where chirality plays a significant role, such as in pharmaceuticals. Overall, this compound is significant in research and development, particularly in the fields of medicinal chemistry and materials science, due to its unique structural features and reactivity.
Formula:C23H43N5O4
Synonyms:- (Dicyclohexylammonium) Salt
- (S)-(-)-2-Azido-6-(boc-amino)hexanoic acid(dicyclohexylammonium) salt
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Found 4 products.
N3-Lys(Boc)
CAS:<p>N3-Lys(Boc)</p>Formula:C11H20N4O4Purity:>99%Color and Shape: white crystalline powderMolecular weight:272.30g/mol(2S)-2-azido-6-{[(tert-butoxy)carbonyl]amino}hexanoic acid
CAS:Formula:C11H20N4O4Purity:99.0%Molecular weight:272.305N3-L-Lys(Boc)-OH
CAS:<p>N3-L-Lys(Boc)-OH is a click chemistry reagent featuring an azide group that can undergo a copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing an alkyne group. Additionally, it can participate in strain-promoted azide-alkyne cycloaddition reactions (SPAAC) with molecules that contain DBCO or BCN groups.</p>Formula:C11H20N4O4Color and Shape:SolidMolecular weight:272.3



