2-(5-phenyl-2H-1,2,3,4-tetraazol-2-yl)acetohydrazide

≥95%

Reagent Code: #197452
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CAS Number 67037-01-8

science Other reagents with same CAS 67037-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.22 g/mol
Formula C₉H₁₀N₆O
badge Registry Numbers
MDL Number MFCD00215520
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. It serves as a building block in heterocyclic chemistry, facilitating the formation of fused ring systems with pharmacological potential. Commonly employed in medicinal chemistry for designing inhibitors targeting specific enzymes due to its ability to coordinate with metal ions in active sites. Also applied in the preparation of hydrazide-hydrazone derivatives that exhibit antioxidant and anti-inflammatory activities. Its structural flexibility allows for easy modification, making it valuable in drug discovery and optimization processes.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,100.00
2-(5-phenyl-2H-1,2,3,4-tetraazol-2-yl)acetohydrazide
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Used as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. It serves as a building block in heterocyclic chemistry, facilitating the formation of fused ring systems with pharmacological potential. Commonly employed in medicinal chemistry for designing inhibitors targeting specific enzymes due to its ability to coordinate with metal ions in active sites. Also applied in the preparation of hydrazide-hydrazone derivatives that

Used as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. It serves as a building block in heterocyclic chemistry, facilitating the formation of fused ring systems with pharmacological potential. Commonly employed in medicinal chemistry for designing inhibitors targeting specific enzymes due to its ability to coordinate with metal ions in active sites. Also applied in the preparation of hydrazide-hydrazone derivatives that exhibit antioxidant and anti-inflammatory activities. Its structural flexibility allows for easy modification, making it valuable in drug discovery and optimization processes.

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