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Benzyl propargyl ether

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Catalog No. TYD-02860Cas No. 4039-82-1
Alias ((Prop-2-yn-1-yloxy)methyl)benzene

Benzyl propargyl ether is a versatile synthetic building block characterized by the linear formula C₆H₅CH₂OCH₂C≡CH and defined by its terminal alkyne functionality, which enables participation in diverse carbon–carbon and carbon–heteroatom bond-forming reactions. Benzyl propargyl ether is widely used in the synthesis of substituted carbocyclic aromatic frameworks, pharmaceutical intermediates, and advanced polymeric materials, Benzyl propargyl ether also serves as a valuable precursor in copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) click chemistry for rapid assembly of functional dendrimers and macromolecules. in carbohydrate chemistry,Benzyl propargyl ether functions as a sterically minimal O-protecting group, and its use at the O-2 position of 4,6-O-benzylidene-protected mannosyl donors enables exceptionally high β-selectivity during challenging glycosylation reactions, supporting efficient synthesis of complex oligosaccharides and glycans.

Benzyl propargyl ether

Benzyl propargyl ether

Copy Product Info
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Catalog No. TYD-02860Alias ((Prop-2-yn-1-yloxy)methyl)benzeneCas No. 4039-82-1
Benzyl propargyl ether is a versatile synthetic building block characterized by the linear formula C₆H₅CH₂OCH₂C≡CH and defined by its terminal alkyne functionality, which enables participation in diverse carbon–carbon and carbon–heteroatom bond-forming reactions. Benzyl propargyl ether is widely used in the synthesis of substituted carbocyclic aromatic frameworks, pharmaceutical intermediates, and advanced polymeric materials, Benzyl propargyl ether also serves as a valuable precursor in copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) click chemistry for rapid assembly of functional dendrimers and macromolecules. in carbohydrate chemistry,Benzyl propargyl ether functions as a sterically minimal O-protecting group, and its use at the O-2 position of 4,6-O-benzylidene-protected mannosyl donors enables exceptionally high β-selectivity during challenging glycosylation reactions, supporting efficient synthesis of complex oligosaccharides and glycans.
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10 mg$70InquiryInquiry
25 mg$113InquiryInquiry
50 mg$163InquiryInquiry
100 mg$239InquiryInquiry
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Description
Benzyl propargyl ether is a versatile synthetic building block characterized by the linear formula C₆H₅CH₂OCH₂C≡CH and defined by its terminal alkyne functionality, which enables participation in diverse carbon–carbon and carbon–heteroatom bond-forming reactions. Benzyl propargyl ether is widely used in the synthesis of substituted carbocyclic aromatic frameworks, pharmaceutical intermediates, and advanced polymeric materials, Benzyl propargyl ether also serves as a valuable precursor in copper(I)-catalyzed azide–alkyne cycloaddition (CuAAC) click chemistry for rapid assembly of functional dendrimers and macromolecules. in carbohydrate chemistry,Benzyl propargyl ether functions as a sterically minimal O-protecting group, and its use at the O-2 position of 4,6-O-benzylidene-protected mannosyl donors enables exceptionally high β-selectivity during challenging glycosylation reactions, supporting efficient synthesis of complex oligosaccharides and glycans.
Synonyms((Prop-2-yn-1-yloxy)methyl)benzene
Chemical Properties
Molecular Weight146.19
FormulaC10H10O
Cas No.4039-82-1
SmilesC#CCOCC=1C=CC=CC1
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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Please enter your animal experiment information in the following box and click Calculate to obtain the stock solution preparation method and in vivo formula preparation method:
TargetMol | Animal experiments For example, if the intended dosage is 10 mg/kg for animals weighing 20 g , with a dosing volume of 100 μL per animal, TargetMol | Animal experiments and a total of 10 animals are to be administered, using a formulation of TargetMol | reagent 10% DMSO+ 40% PEG300+ 5% Tween 80+ 45% Saline/PBS/ddH2O , the resulting working solution concentration would be 2 mg/mL.
Stock Solution Preparation:

Dissolve 2 mg of the compound in 100 μL DMSOTargetMol | reagent to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.

Preparation of the In Vivo Formulation:

1) Add 100 μL of the DMSOTargetMol | reagent stock solution to 400 μL PEG300TargetMol | reagent and mix thoroughly until the solution becomes clear.

2) Add 50 μL Tween 80 and mix well until fully clarified.

3) Add 450 μL Saline,PBS or ddH2OTargetMol | reagent and mix thoroughly until a homogeneous solution is obtained.

This example is provided solely to demonstrate the use of the In Vivo Formulation Calculator and does not constitute a recommended formulation for any specific compound. Please select an appropriate dissolution and formulation strategy based on your experimental model and route of administration.
All co-solvents required for this protocol, includingDMSO, PEG300/PEG400, Tween 80, SBE-β-CD, and Corn oil, are available for purchase on the TargetMol website.
1 Enter information below:
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2 Enter the in vivo formulation:
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Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc
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