5-(4-Chlorophenyl)-1,3,4-oxadiazole-2-thiol

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Reagent Code: #162703
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CAS Number 23766-28-1

science Other reagents with same CAS 23766-28-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.66 g/mol
Formula C₈H₅ClN₂OS
badge Registry Numbers
MDL Number MFCD00227512
thermostat Physical Properties
Melting Point 171-175 °C
Boiling Point 277 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.53 g/cm3
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimicrobial (including antibacterial and antiviral), anti-inflammatory, and anti-cancer agents. Exhibits potential in agrochemical applications as a building block for novel pesticides due to its heterocyclic structure. Also employed in coordination chemistry, acting as a ligand for metal ions in catalytic systems. In organic synthesis, it facilitates reactions to form carbon-sulfur or carbon-nitrogen bonds for creating complex structures. Its derivatives are explored in materials science for optoelectronic applications owing to electron-transport properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,560.00
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5-(4-Chlorophenyl)-1,3,4-oxadiazole-2-thiol
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimicrobial (including antibacterial and antiviral), anti-inflammatory, and anti-cancer agents. Exhibits potential in agrochemical applications as a building block for novel pesticides due to its heterocyclic structure. Also employed in coordination chemistry, acting as a ligand for metal ions in catalytic systems. In organic synthesis, it facilitates reactions to form carbon-sulfur or carbon-nitrog

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimicrobial (including antibacterial and antiviral), anti-inflammatory, and anti-cancer agents. Exhibits potential in agrochemical applications as a building block for novel pesticides due to its heterocyclic structure. Also employed in coordination chemistry, acting as a ligand for metal ions in catalytic systems. In organic synthesis, it facilitates reactions to form carbon-sulfur or carbon-nitrogen bonds for creating complex structures. Its derivatives are explored in materials science for optoelectronic applications owing to electron-transport properties.

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