Tert-butyl 4-amino-1H-indazole-1-carboxylate

98%

Reagent Code: #240153
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CAS Number 801315-74-2

science Other reagents with same CAS 801315-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.27 g/mol
Formula C₁₂H₁₅N₃O₂
badge Registry Numbers
MDL Number MFCD11052618
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating bioactive molecules. Commonly employed in medicinal chemistry research to build indazole-based scaffolds that exhibit anti-inflammatory, antiviral, or antitumor activity. Also utilized in the preparation of PROTACs (proteolysis-targeting chimeras) due to its favorable reactivity and stability in multi-step organic transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿590.00
inventory 250mg
10-20 days ฿860.00
inventory 5g
10-20 days ฿10,310.00
inventory 10g
10-20 days ฿20,570.00
inventory 1g
10-20 days ฿2,300.00

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Tert-butyl 4-amino-1H-indazole-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating bioactive molecules. Commonly employed in medicinal chemistry research to build indazole-based scaffolds that exhibit anti-inflammatory, antiviral, or antitumor activity. Also utilized in the preparation of PROTACs (proteolysis-targeting chimeras) due to its favorable reactivity a

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating bioactive molecules. Commonly employed in medicinal chemistry research to build indazole-based scaffolds that exhibit anti-inflammatory, antiviral, or antitumor activity. Also utilized in the preparation of PROTACs (proteolysis-targeting chimeras) due to its favorable reactivity and stability in multi-step organic transformations.

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