(5-Ethynylpyridin-2-yl)methanol

≥95%

Reagent Code: #57361
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CAS Number 1033705-77-9

science Other reagents with same CAS 1033705-77-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 133.15 g/mol
Formula C₈H₇NO
badge Registry Numbers
MDL Number MFCD11520016
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the creation of more complex molecules. Its ethynyl group makes it particularly valuable in click chemistry reactions, enabling the formation of triazole derivatives through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This property is exploited in the development of pharmaceuticals, where it can be used to synthesize drug candidates with potential therapeutic applications. Additionally, its pyridine moiety allows it to act as a ligand in coordination chemistry, facilitating the formation of metal complexes that are useful in catalysis and material science. The hydroxyl group further enhances its reactivity, making it a suitable intermediate for the preparation of esters, ethers, and other functionalized compounds. Overall, this chemical plays a significant role in advancing research and development across various scientific disciplines.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,200.00
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(5-Ethynylpyridin-2-yl)methanol
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the creation of more complex molecules. Its ethynyl group makes it particularly valuable in click chemistry reactions, enabling the formation of triazole derivatives through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This property is exploited in the development of pharmaceuticals, where it can be used to synthesize drug candidates with potential therapeutic applications. Add

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the creation of more complex molecules. Its ethynyl group makes it particularly valuable in click chemistry reactions, enabling the formation of triazole derivatives through copper-catalyzed azide-alkyne cycloaddition (CuAAC). This property is exploited in the development of pharmaceuticals, where it can be used to synthesize drug candidates with potential therapeutic applications. Additionally, its pyridine moiety allows it to act as a ligand in coordination chemistry, facilitating the formation of metal complexes that are useful in catalysis and material science. The hydroxyl group further enhances its reactivity, making it a suitable intermediate for the preparation of esters, ethers, and other functionalized compounds. Overall, this chemical plays a significant role in advancing research and development across various scientific disciplines.

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