6-Nitro-1H-indazol-4-carboxylic acid

95%

Reagent Code: #86858
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CAS Number 885519-61-9

science Other reagents with same CAS 885519-61-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.143 g/mol
Formula C₈H₅N₃O₄
badge Registry Numbers
MDL Number MFCD07781677
thermostat Physical Properties
Boiling Point 525.1±35.0 °C
inventory_2 Storage & Handling
Density 1.733±0.06 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structural features make it a valuable building block for developing potential drug candidates, especially in the design of inhibitors for therapeutic applications. Researchers often employ it in the creation of compounds aimed at treating diseases such as cancer, inflammation, or microbial infections. Additionally, its nitro and carboxylic acid functional groups allow for further chemical modifications, enabling the development of diverse derivatives with tailored properties for specific biological targets.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,499.00
inventory 250mg
10-20 days ฿21,960.00

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6-Nitro-1H-indazol-4-carboxylic acid
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzymes or receptors. Its structural features make it a valuable building block for developing potential drug candidates, especially in the design of inhibitors for therapeutic applications. Researchers often employ it in the creation of compounds aimed at treating diseases such as cancer, inflammation, or microbial infections. Additionally, its nitro and carboxylic acid functional groups allow for further chemical modifications, enabling the development of diverse derivatives with tailored properties for specific biological targets.
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