methyl 4-(4-azidobutyl)benzoate

99%

Reagent Code: #209286
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CAS Number 141019-01-4

science Other reagents with same CAS 141019-01-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.27 g/mol
Formula C₁₂H₁₅N₃O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in click chemistry applications, particularly in bioconjugation and labeling of biomolecules. The azide group readily participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient attachment to alkyne-functionalized compounds. This makes it valuable in drug discovery, proteomics, and development of fluorescent probes. Also employed in polymer science to introduce aromatic ester moieties into macromolecular structures via modular coupling reactions. Its bifunctional nature allows for linker construction in targeted delivery systems and functional material design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,420.00
500mg
10-20 days ฿4,760.00
1g
10-20 days ฿8,730.00
5g
10-20 days ฿25,650.00
methyl 4-(4-azidobutyl)benzoate
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Used in click chemistry applications, particularly in bioconjugation and labeling of biomolecules. The azide group readily participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient attachment to alkyne-functionalized compounds. This makes it valuable in drug discovery, proteomics, and development of fluorescent probes. Also employed in polymer science to introduce aromatic ester moieties into macromolecular structures via modular coupling reactions. Its bifunctiona

Used in click chemistry applications, particularly in bioconjugation and labeling of biomolecules. The azide group readily participates in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, enabling efficient attachment to alkyne-functionalized compounds. This makes it valuable in drug discovery, proteomics, and development of fluorescent probes. Also employed in polymer science to introduce aromatic ester moieties into macromolecular structures via modular coupling reactions. Its bifunctional nature allows for linker construction in targeted delivery systems and functional material design.

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