1454816-10-4

Fmoc-L-Tyr(2-azidoethyl)-OH Chemical Structure
1454816-10-4

Chemical Structure

Fmoc-L-Tyr(2-azidoethyl)-OH

  • CAS No.: 1454816-10-4
  • Formula:C26H24N4O5
  • Molecular Weight:472.49

IUPAC Name: (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-(2-azidoethoxy)phenyl)propanoic acid

InChIKey: OEXYEZJGYOWMNJ-DEOSSOPVSA-N

SMILES: [N-]=[N+]=NCCOC(C=C1)=CC=C1C[C@@H](C(O)=O)NC(OCC2C3=CC=CC=C3C4=CC=CC=C42)=O

Biological Activity: Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters[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-151687
Fmoc-L-Tyr(2-azidoethyl)-OH Fmoc-L-Tyr(2-azidoethyl)-OH is a click chemistry reagent containing an azide group. Fmoc-L-Tyr(2-azidoethyl)-OH is unnatural Fmoc-protected Tyrosine derivative bears an azidoethyl substitution as reactive handle e.g. for biorthogonal conjugations, via a Cu(I)-catalyzed 1,3-dipolar Click cycloaddition with alkynes. And azido-UAAs can be employed as IR reporters. 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