N,N-Dimethyl-1H-indazol-5-amine

≥95%

Reagent Code: #218197
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CAS Number 945264-96-0

science Other reagents with same CAS 945264-96-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.20 g/mol
Formula C₉H₁₁N₃
badge Registry Numbers
MDL Number MFCD17392852
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used primarily in organic synthesis, this compound serves as a building block in the development of pharmaceuticals, particularly in the design of kinase inhibitors and bioactive molecules targeting inflammation and cancer. Its indazole core with a dimethylamino group enhances binding affinity to certain enzyme active sites, making it valuable in medicinal chemistry research. It is also employed in the preparation of fluorescent probes and agrochemical intermediates due to its electron-donating properties and structural stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,290.00
inventory 250mg
10-20 days ฿8,580.00

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N,N-Dimethyl-1H-indazol-5-amine
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Used primarily in organic synthesis, this compound serves as a building block in the development of pharmaceuticals, particularly in the design of kinase inhibitors and bioactive molecules targeting inflammation and cancer. Its indazole core with a dimethylamino group enhances binding affinity to certain enzyme active sites, making it valuable in medicinal chemistry research. It is also employed in the preparation of fluorescent probes and agrochemical intermediates due to its electron-donating propertie

Used primarily in organic synthesis, this compound serves as a building block in the development of pharmaceuticals, particularly in the design of kinase inhibitors and bioactive molecules targeting inflammation and cancer. Its indazole core with a dimethylamino group enhances binding affinity to certain enzyme active sites, making it valuable in medicinal chemistry research. It is also employed in the preparation of fluorescent probes and agrochemical intermediates due to its electron-donating properties and structural stability.

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