2086689-04-3

N-(Azido-PEG2)-N-Fluorescein-PEG3-acid Chemical Structure
2086689-04-3

Chemical Structure

N-(Azido-PEG2)-N-Fluorescein-PEG3-acid

  • CAS No.: 2086689-04-3
  • Formula:C36H41N5O12S
  • Molecular Weight:767.80

IUPAC Name: 1-azido-9-((3',6'-dihydroxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthen]-5-yl)carbamothioyl)-3,6,12,15,18-pentaoxa-9-azahenicosan-21-oic acid

InChIKey: PMJYXCRDKLEIKK-UHFFFAOYSA-N

SMILES: O=C(O)CCOCCOCCOCCN(CCOCCOCCN=[N+]=[N-])C(NC1=CC2=C(C3(C4=C(OC5=C3C=CC(O)=C5)C=C(O)C=C4)OC2=O)C=C1)=S

Biological Activity: N-(Azido-PEG2)-N-Fluorescein-PEG3-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. N-(Azido-PEG2)-N-Fluorescein-PEG3-acid 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-140544
N-(Azido-PEG2)-N-Fluorescein-PEG3-acid N-(Azido-PEG2)-N-Fluorescein-PEG3-acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. N-(Azido-PEG2)-N-Fluorescein-PEG3-acid 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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