4-(1H-1,2,3-Triazol-1-yl)benzoic acid

98%

Reagent Code: #46088
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CAS Number 216959-87-4

science Other reagents with same CAS 216959-87-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.1708 g/mol
Formula C₉H₇N₃O₂
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Storage room temperature

description Product Description

This compound 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 structure, featuring both a triazole ring and a benzoic acid group, makes it valuable in the development of pharmaceuticals, particularly in the design of drugs targeting specific biological pathways. Additionally, it is employed in the synthesis of materials with potential applications in organic electronics and photovoltaics, due to its ability to facilitate charge transport. The compound is also explored in the development of metal-organic frameworks (MOFs) and other advanced materials, where its functional groups can enhance structural stability and reactivity.

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Test Parameter Specification
Appearance White to Off-White to Yellow Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,259.00

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4-(1H-1,2,3-Triazol-1-yl)benzoic acid
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This compound 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 structure, featuring both a triazole ring and a benzoic acid group, makes it valuable in the development of pharmaceuticals, particularly in the design of drugs targeting specific biological pathways. Additionally, it is employed in the synthesis of materials with potential applications in organic electronics and photovoltaics, due to its ability to facilitate charge transport. The compound is also explored in the development of metal-organic frameworks (MOFs) and other advanced materials, where its functional groups can enhance structural stability and reactivity.
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