4-(2H-1,2,3-Triazol-2-yl)benzaldehyde

97%

Reagent Code: #118539
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CAS Number 179056-04-3

science Other reagents with same CAS 179056-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.17 g/mol
Formula C₉H₇N₃O
badge Registry Numbers
MDL Number MFCD08669904
thermostat Physical Properties
Boiling Point 356.824°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis as a versatile building block for creating complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of triazole-containing compounds, which are known for their antimicrobial, antifungal, and anticancer properties. The aldehyde group allows for further functionalization, enabling the creation of Schiff bases, heterocycles, and other derivatives. Additionally, it is employed in materials science for designing functional polymers and coatings with specific chemical or physical properties. Its triazole moiety also makes it useful in click chemistry reactions, facilitating efficient and selective bond formations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,986.00
inventory 1g
10-20 days ฿20,070.00
inventory 250mg
10-20 days ฿8,001.00

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4-(2H-1,2,3-Triazol-2-yl)benzaldehyde
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Used in organic synthesis as a versatile building block for creating complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of triazole-containing compounds, which are known for their antimicrobial, antifungal, and anticancer properties. The aldehyde group allows for further functionalization, enabling the creation of Schiff bases, heterocycles, and other derivatives. Additionally, it is employed in materials scien

Used in organic synthesis as a versatile building block for creating complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the preparation of triazole-containing compounds, which are known for their antimicrobial, antifungal, and anticancer properties. The aldehyde group allows for further functionalization, enabling the creation of Schiff bases, heterocycles, and other derivatives. Additionally, it is employed in materials science for designing functional polymers and coatings with specific chemical or physical properties. Its triazole moiety also makes it useful in click chemistry reactions, facilitating efficient and selective bond formations.

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