7-Nitro-1H-indazole

97 %

Reagent Code: #110829
label
Alias 7-NI
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CAS Number 2942-42-9

science Other reagents with same CAS 2942-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.14 g/mol
Formula C₇H₅N₃O₂
badge Registry Numbers
EC Number 220-934-4
MDL Number MFCD00022789
thermostat Physical Properties
Melting Point 185-186°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily in pharmaceutical research, it serves as a key intermediate in the synthesis of various biologically active compounds. Its nitro group makes it a valuable precursor for developing potential drugs targeting enzymes and receptors. In medicinal chemistry, it is employed to create molecules with anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is utilized in organic synthesis to construct complex heterocyclic structures, which are essential in drug discovery and development. Its role in experimental studies often focuses on optimizing drug efficacy and understanding biochemical pathways.

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Test Parameter Specification
Melting Point 184-189
Purity (HPLC) 96.5-100
Appearance Yellow to Brown
Proton NMR Spectrum Conforms To Structure
Solubility Clear Yellow To Orange

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,079.00
inventory 1g
10-20 days ฿693.00

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7-Nitro-1H-indazole
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Used primarily in pharmaceutical research, it serves as a key intermediate in the synthesis of various biologically active compounds. Its nitro group makes it a valuable precursor for developing potential drugs targeting enzymes and receptors. In medicinal chemistry, it is employed to create molecules with anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is utilized in organic synthesis to construct complex heterocyclic structures, which are essential in drug discovery and development. Its role in experimental studies often focuses on optimizing drug efficacy and understanding biochemical pathways.
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