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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

😃Good
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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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
ColorTransparent
AppearanceLiquid
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year

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Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
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