2086689-00-9

N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) Chemical Structure
2086689-00-9

Chemical Structure

N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester)

  • CAS No.: 2086689-00-9
  • Formula:C26H48N4O10
  • Molecular Weight:576.68

IUPAC Name: tert-butyl 1-azido-14-((3-(tert-butoxy)-3-oxopropoxy)methyl)-12-oxo-3,6,9,16-tetraoxa-13-azanonadecan-19-oate

InChIKey: MFAWTCNLWLJEKI-UHFFFAOYSA-N

SMILES: O=C(OC(C)(C)C)CCOCC(COCCC(OC(C)(C)C)=O)NC(CCOCCOCCOCCN=[N+]=[N-])=O

Biological Activity: N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) 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. Nom du produit Pureté Description Pricing
HY-140873
N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-(Azido-PEG3)-N-bis(PEG1-t-butyl ester) 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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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

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

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References