1932403-71-8

N3-L-Dab(Boc)-OH Chemical Structure
1932403-71-8

Chemical Structure

N3-L-Dab(Boc)-OH

  • CAS No.: 1932403-71-8
  • Formula:C9H16N4O4
  • Molecular Weight:244.25

IUPAC Name: (S)-2-azido-4-((tert-butoxycarbonyl)amino)butanoic acid

InChIKey: JLMWKZYQNHSSAD-LURJTMIESA-N

SMILES: CC(C)(C)OC(NCC[C@@H](C(O)=O)N=[N+]=[N-])=O

Biological Activity: N3-L-Dab(Boc)-OH is a click chemistry reagent containing an azide group. N3-L-Dab(Boc)-OH can be used for the research of various biochemical[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.

Cat. No. Product Name Purity Description Pricing
HY-151735
N3-L-Dab(Boc)-OH N3-L-Dab(Boc)-OH is a click chemistry reagent containing an azide group. N3-L-Dab(Boc)-OH can be used for the research of various biochemical. 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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References