1H-Indazole-6-carbohydrazide

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Reagent Code: #197312
label
Alias 2H-indazole e-6-carbohydrazide
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CAS Number 1086392-18-8

science Other reagents with same CAS 1086392-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.18 g/mol
Formula C₈H₈N₄O
badge Registry Numbers
MDL Number MFCD11506091
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly kinase inhibitors with potential anticancer properties. It serves as a building block for developing molecules that modulate cellular signaling pathways. Its hydrazide group allows for easy derivatization, enabling the formation of Schiff bases and other functionalized derivatives used in drug discovery. Also explored in the design of anti-inflammatory and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and aromatic interactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿6,290.00
inventory 1g
10-20 days ฿13,170.00
inventory 5g
10-20 days ฿50,380.00
inventory 25g
10-20 days ฿84,140.00
1H-Indazole-6-carbohydrazide
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Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly kinase inhibitors with potential anticancer properties. It serves as a building block for developing molecules that modulate cellular signaling pathways. Its hydrazide group allows for easy derivatization, enabling the formation of Schiff bases and other functionalized derivatives used in drug discovery. Also explored in the design of anti-inflammatory and antimicrobial agents due to its ability to

Used in pharmaceutical research as a key intermediate in the synthesis of bioactive compounds, particularly kinase inhibitors with potential anticancer properties. It serves as a building block for developing molecules that modulate cellular signaling pathways. Its hydrazide group allows for easy derivatization, enabling the formation of Schiff bases and other functionalized derivatives used in drug discovery. Also explored in the design of anti-inflammatory and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and aromatic interactions.

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