1333231-26-7

N3-L-Lys(Mtt)-OH Chemical Structure
1333231-26-7

Chemical Structure

N3-L-Lys(Mtt)-OH

  • CAS No.: 1333231-26-7
  • Formula:C26H28N4O2
  • Molecular Weight:428.53

IUPAC Name: (S)-2-azido-6-((diphenyl(p-tolyl)methyl)amino)hexanoic acid

InChIKey: KBXSFBJXJSKJBY-DEOSSOPVSA-N

SMILES: [N-]=[N+]=N[C@H](C(O)=O)CCCCNC(C1=CC=CC=C1)(C2=CC=CC=C2)C3=CC=C(C=C3)C

Biological Activity: N3-L-Lys(Mtt)-OH is a click chemistry reagent containing an azide group. N3-L-Lys(Mtt)-OH can introduce azide functions into the amino acid building block of peptide sequences at the N-terminal position. 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-151678
N3-L-Lys(Mtt)-OH N3-L-Lys(Mtt)-OH is a click chemistry reagent containing an azide group. N3-L-Lys(Mtt)-OH can introduce azide functions into the amino acid building block of peptide sequences at the N-terminal position. 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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