2-((1H-Benzo[d]imidazol-2-yl)thio)acetohydrazide

95%

Reagent Code: #197008
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CAS Number 30065-27-1

science Other reagents with same CAS 30065-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.27 g/mol
Formula C₉H₁₀N₄OS
badge Registry Numbers
MDL Number MFCD00171027
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. Exhibits potential in the design of new drug candidates due to its ability to interact with microbial enzymes and disrupt cell function. Also employed in coordination chemistry as a ligand for metal ions, aiding in the creation of metal-based therapeutic complexes. Its hydrazide group allows for easy modification, making it valuable in the preparation of heterocyclic derivatives with enhanced biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,140.00
5g
10-20 days ฿5,580.00
25g
10-20 days ฿24,230.00
2-((1H-Benzo[d]imidazol-2-yl)thio)acetohydrazide
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. Exhibits potential in the design of new drug candidates due to its ability to interact with microbial enzymes and disrupt cell function. Also employed in coordination chemistry as a ligand for metal ions, aiding in the creation of metal-based therapeutic complexes. Its hydrazide group allows for easy modification, making it valuable in the

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly in the development of antimicrobial and antifungal agents. Exhibits potential in the design of new drug candidates due to its ability to interact with microbial enzymes and disrupt cell function. Also employed in coordination chemistry as a ligand for metal ions, aiding in the creation of metal-based therapeutic complexes. Its hydrazide group allows for easy modification, making it valuable in the preparation of heterocyclic derivatives with enhanced biological activity.

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