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Organometallic compounds contain direct bonds between carbon atoms and metal atoms/ions and play roles as homogeneous catalysts and stoichiometric reagents in reactions; available in various chemical compositions, quantities, purities, and reagent grades.
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N-(Amino-PEG3)-N-bis(PEG4-Boc) is a PEG-based PROTAC linker. It can be used in the synthesis of PROTACs and has applications in cancer-programmed cell death.
PEG-based PROTAC linker
Used in the synthesis of PROTACs
Applications in cancer-programmed cell death
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Tos-PEG3 is a PEG-based PROTAC linker that can be utilized in the synthesis of PROTACs. It can also be used for the synthesis of 3'-aminooxy oligonucleotides solid supports.
Utilized in the synthesis of PROTACs.
Can be used for the synthesis of 3'-aminooxy oligonucleotides solid supports.
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Azido-PEG5-azide is a PEG-based PROTAC linker primarily used in the synthesis of PROTACs. It functions as a versatile click chemistry reagent, capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. Additionally, it can participate in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
Used in the synthesis of PROTACs
Functions as a click chemistry reagent
Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne groups
Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) with DBCO or BCN groups
For research use only
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BCN-exo-PEG3-NH2 is a PEG-based PROTAC linker primarily used in the synthesis of PROTACs. It acts as a click chemistry reagent, featuring a BCN group that can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules containing azide groups. PROTACs leverage the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
Purity: 99.94%
Molecular weight: 368.47
Chemical formula: C19H32N2O5
CAS number: 1841134-72-2
Appearance: Colorless to light yellow liquid
Density: 1.14±0.1 g/cm3
Used in PROTAC synthesis
Contains a BCN group for SPAAC reactions
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N3-PEG3-CH2CH2-Boc is a Boc-protected, azide-terminated PEG3 linker used in conjugation chemistry for synthesizing PROTACs and antibody-drug conjugates. It contains a three-unit polyethylene glycol spacer with an azide functional group that enables click chemistry reactions such as copper-catalyzed azide-alkyne cycloaddition (CuAAC) and strain-promoted azide-alkyne cycloaddition (SPAAC).
Boc-protected azide terminus for selective conjugation.
Three-unit PEG spacer provides flexibility and improves solubility.
Compatible with CuAAC and SPAAC click reaction methodologies.
High purity suitable for synthetic applications (≥98.0%).
Available in multiple pack sizes, including 250 MG.
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N-(Azido-PEG3)-N-(PEG2-NH-Boc)-PEG3-acid is a PEG-based linker designed for use in click chemistry and bioconjugation workflows. It features a terminal azide and orthogonally protected amine, providing versatility for PROTAC assembly and other synthetic applications.
Terminal azide for copper-catalyzed azide-alkyne cycloaddition (CuAAC).
Compatible with strain-promoted alkyne-azide cycloaddition (SPAAC).
PEG3 spacer provides flexibility and improved solubility.
Boc-protected amine on PEG2 enables selective deprotection and further modification.
Carboxylic acid terminus allows conjugation via standard amide coupling.
High purity suitable for synthetic and bioconjugation workflows.
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