2093153-07-0

N-(Azido-PEG2)-N-Boc-PEG3-Boc Chemical Structure
2093153-07-0

Chemical Structure

N-(Azido-PEG2)-N-Boc-PEG3-Boc

  • CAS No.: 2093153-07-0
  • Formula:C24H46N4O9
  • Molecular Weight:534.64

IUPAC Name: tert-butyl 1-azido-9-(tert-butoxycarbonyl)-3,6,12,15,18-pentaoxa-9-azahenicosan-21-oate

InChIKey: YULNOPFYPKAAPI-UHFFFAOYSA-N

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

Biological Activity: N-(Azido-PEG2)-N-Boc-PEG3-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG2)-N-Boc-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-140562
N-(Azido-PEG2)-N-Boc-PEG3-Boc N-(Azido-PEG2)-N-Boc-PEG3-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-(Azido-PEG2)-N-Boc-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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