2-(1H-1,2,3-Triazol-1-yl)ethanol

97%

Reagent Code: #196859
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CAS Number 74731-63-8

science Other reagents with same CAS 74731-63-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 113.12 g/mol
Formula C₄H₇N₃O
badge Registry Numbers
MDL Number MFCD03840805
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of antifungal and antiviral agents. Its triazole ring enables click chemistry reactions, making it valuable in drug discovery and bioconjugation. Also employed in the development of functionalized polymers and smart materials due to its ability to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. Additionally, it serves as a building block in agrochemicals and corrosion inhibitors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,400.00
inventory 250mg
10-20 days ฿7,470.00
inventory 5g
10-20 days ฿78,740.00
inventory 1g
10-20 days ฿20,130.00
2-(1H-1,2,3-Triazol-1-yl)ethanol
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Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of antifungal and antiviral agents. Its triazole ring enables click chemistry reactions, making it valuable in drug discovery and bioconjugation. Also employed in the development of functionalized polymers and smart materials due to its ability to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. Additionally, it serves as a building block in agrochemicals and corrosion inhibitors.

Used as a key intermediate in pharmaceutical synthesis, particularly in the preparation of antifungal and antiviral agents. Its triazole ring enables click chemistry reactions, making it valuable in drug discovery and bioconjugation. Also employed in the development of functionalized polymers and smart materials due to its ability to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. Additionally, it serves as a building block in agrochemicals and corrosion inhibitors.

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