2098497-30-2
Chemical Structure
Boc-L-Lys(N3)-OH (CHA)
- CAS No.: 2098497-30-2
- Formula:C17H33N5O4
- Molecular Weight:371.48
IUPAC Name: cyclohexanamine N2-(tert-butoxycarbonyl)-N6-diazo-L-lysinate
InChIKey: NHHYBEBTGVUZET-QRPNPIFTSA-N
SMILES: NC1CCCCC1.CC(C)(C)OC(N[C@H](C(O)=O)CCCCN=[N+]=[N-])=O
Biological Activity: Boc-L-Lys(N3)-OH CHA is a click chemistry reagent containing an azide[1]. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups.
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Boc-L-Lys(N3)-OH (CHA) | Boc-L-Lys(N3)-OH CHA is a click chemistry reagent containing an azide. It contains an azide group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing alkyne groups. It can also undergo ring strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing DBCO or BCN groups. | |||||||||||||||||||||
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