2093152-85-1

N-Azido-PEG4-N-Boc-N-PEG3-Boc Chemical Structure
2093152-85-1

Chemical Structure

N-Azido-PEG4-N-Boc-N-PEG3-Boc

  • CAS No.: 2093152-85-1
  • Formula:C28H54N4O11
  • Molecular Weight:622.75

IUPAC Name: tert-butyl 1-azido-15-(tert-butoxycarbonyl)-3,6,9,12,18,21,24-heptaoxa-15-azaheptacosan-27-oate

InChIKey: NWHTZGJNDFXFNW-UHFFFAOYSA-N

SMILES: O=C(OC(C)(C)C)N(CCOCCOCCOCCOCCN=[N+]=[N-])CCOCCOCCOCCC(OC(C)(C)C)=O

Biological Activity: N-Azido-PEG4-N-Boc-N-PEG3-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-Azido-PEG4-N-Boc-N-PEG3-Boc is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.

Cat. No. Product Name Purity Description Pricing
HY-140566
N-Azido-PEG4-N-Boc-N-PEG3-Boc N-Azido-PEG4-N-Boc-N-PEG3-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-Azido-PEG4-N-Boc-N-PEG3-Boc is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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