N'-((2-Methyl-1H-indol-3-yl)methylene)thiophene-2-carbohydrazide

98%

Reagent Code: #215852
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CAS Number 113144-90-4

science Other reagents with same CAS 113144-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.35 g/mol
Formula C₁₅H₁₃N₃OS
inventory_2 Storage & Handling
Density 1.32±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its structure supports the development of indole-based derivatives known for inhibiting specific enzyme pathways in tumor cells. Also employed in the design of novel hydrazide-hydrazone compounds with observed activity against resistant microbial strains. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to form stable complexes with metal ions, enhancing pharmacological potential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,060.00
inventory 250mg
10-20 days ฿32,410.00

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N'-((2-Methyl-1H-indol-3-yl)methylene)thiophene-2-carbohydrazide
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Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its structure supports the development of indole-based derivatives known for inhibiting specific enzyme pathways in tumor cells. Also employed in the design of novel hydrazide-hydrazone compounds with observed activity against resistant microbial strains. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to

Used as a key intermediate in the synthesis of bioactive compounds, particularly in pharmaceutical research targeting anticancer and antimicrobial agents. Its structure supports the development of indole-based derivatives known for inhibiting specific enzyme pathways in tumor cells. Also employed in the design of novel hydrazide-hydrazone compounds with observed activity against resistant microbial strains. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to form stable complexes with metal ions, enhancing pharmacological potential.

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