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

Catalog No.: A83564
PROTAC Linker
N-(Azido-PEG2)-N-Boc-PEG3-Boc is a PEG-based linker designed for use in the synthesis of PROTACs, with a primary mechanism involving click chemistry. It features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) groups, enhancing its utility in diverse chemical biology applications. The compound provides a versatile tool for researchers in drug development and targeted protein degradation studies.
Grouped product items
Size Price Stock Qty
2mg
$30.00
In stock
5mg
$45.00
In stock
100mg
$120.00
In stock
250mg
$280.00
In stock
500mg
$560.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionN-(Azido-PEG2)-N-Boc-PEG3-Boc is a PEG-based linker designed for use in the synthesis of PROTACs, with a primary mechanism involving click chemistry. It features an azide functional group that facilitates copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-containing molecules. Additionally, it supports strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with dibenzocyclooctyne (DBCO) or bicyclononyne (BCN) groups, enhancing its utility in diverse chemical biology applications. The compound provides a versatile tool for researchers in drug development and targeted protein degradation studies.
Product Information
Catalog NumA83564
FormulaC24H46N4O9
Molecular Weight534.64
CAS Number2093153-07-0
SMILESO=C(OC(C)(C)C)N(CCOCCOCCN=[N+]=[N-])CCOCCOCCOCCC(OC(C)(C)C)=O
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