1620410-04-9

Boc-D-Lys(N3)-OH Chemical Structure
1620410-04-9

Chemical Structure

Boc-D-Lys(N3)-OH

  • CAS No.: 1620410-04-9
  • Formula:C11H20N4O4
  • Molecular Weight:272.30

IUPAC Name: N2-(tert-butoxycarbonyl)-N6-diazo-D-lysine

InChIKey: SKRPDWWWUARZIW-MRVPVSSYSA-N

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

Biological Activity: Boc-D-Lys(N3)-OH is a Boc-protected amino acid derivative, can be used as a click chemistry reagent and an intermediate for synthesis of linkers[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-151703
Boc-D-Lys(N3)-OH Boc-D-Lys(N3)-OH is a Boc-protected amino acid derivative, can be used as a click chemistry reagent and an intermediate for synthesis of linkers. 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.

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

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References