2112731-81-2

N-(Azido-PEG2)-N-bis(PEG4-Boc) Chemical Structure
2112731-81-2

Chemical Structure

N-(Azido-PEG2)-N-bis(PEG4-Boc)

  • CAS No.: 2112731-81-2
  • Formula:C36H70N4O14
  • Molecular Weight:782.96

IUPAC Name: di-tert-butyl 16-(2-(2-(2-azidoethoxy)ethoxy)ethyl)-4,7,10,13,19,22,25,28-octaoxa-16-azahentriacontanedioate

InChIKey: QMUHVUPHHRSFNU-UHFFFAOYSA-N

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

Biological Activity: N-(Azido-PEG2)-N-bis(PEG4-Boc) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG2)-N-bis(PEG4-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-140867
N-(Azido-PEG2)-N-bis(PEG4-Boc) N-(Azido-PEG2)-N-bis(PEG4-Boc) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-(Azido-PEG2)-N-bis(PEG4-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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