944560-99-0

Propargyl-PEG6-alcohol Chemical Structure
944560-99-0

Chemical Structure

Propargyl-PEG6-alcohol

  • CAS No.: 944560-99-0
  • Formula:C15H28O7
  • Molecular Weight:320.38

IUPAC Name: 3,6,9,12,15,18-hexaoxahenicos-20-yn-1-ol

InChIKey: USWWECGLRVWCRJ-UHFFFAOYSA-N

SMILES: C#CCOCCOCCOCCOCCOCCOCCO

Biological Activity: Propargyl-PEG6-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs[1]. Propargyl-PEG6-alcohol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.

Cat. No. Product Name Purity Description Pricing
HY-130382
Propargyl-PEG6-alcohol 97.0% Propargyl-PEG6-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG6-alcohol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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HY-120918
NH2-PEG7 98.0% NH2-PEG7 is a PROTAC linker, which refers to the PEG composition. NH2-PEG7 can be used in the synthesis of PROTAC PARP1 degraders, such as iRucaparib-AP6 (HY-130644).
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HY-130147
Propargyl-PEG5-OH 97.0% Propargyl-PEG5-OH is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG5-OH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-130180
Propargyl-PEG6-NH2 99.69% Propargyl-PEG6-NH2 is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG6-NH2 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-130378
Propargyl-PEG7-alcohol 97.0% Propargyl-PEG7-alcohol is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG7-alcohol is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-130386
Propargyl-PEG6-acid Propargyl-PEG6-acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs. Propargyl-PEG6-acid is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs). Propargyl-PEG6-acid is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-133193
Bis-propargyl-PEG5 98.0% Bis-propargyl-PEG5 is a PEG-based PROTAC linker used in the synthesis of PROTACs. Bis-propargyl-PEG5 is used for the synthesis of carbohydrate receptors (SCRs) with anti-Zika activity. Bis-propargyl-PEG5 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-135917
Propargyl-PEG6-SH Propargyl-PEG6-SH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Propargyl-PEG6-SH is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-138321
Propargyl-PEG6-Br Propargyl-PEG6-Br is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. Propargyl-PEG6-Br is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-138719
m-PEG5-Propyne m-PEG5-Propyne is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. m-PEG5-Propyne is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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HY-141231
Heptaethylene glycol 97.0% Heptaethylene glycol is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
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References