1-(1H-Indazol-1-yl)ethanone

95%

Reagent Code: #195616
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CAS Number 13436-49-2

science Other reagents with same CAS 13436-49-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.17 g/mol
Formula C₉H₈N₂O
badge Registry Numbers
MDL Number MFCD16657163
thermostat Physical Properties
Boiling Point 306.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to participate in condensation and cyclization reactions. Commonly employed in medicinal chemistry for modifying indazole-based scaffolds to enhance drug potency and selectivity. Also utilized in the creation of novel psychoactive substances for research purposes, though not approved for human use. Its structural features make it valuable in the design of small molecule therapeutics targeting neurological and inflammatory disorders.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿412.50
inventory 5g
10-20 days ฿1,589.50
inventory 10g
10-20 days ฿3,179.00

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1-(1H-Indazol-1-yl)ethanone
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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. It serves as a building block in the preparation of bioactive molecules due to its ability to participate in condensation and cyclization reactions. Commonly employed in medicinal chemistry for modifying indazole-based scaffolds to enhance drug potency and selectivity. Also utilized in the creation of novel psychoactive substances for research purposes, thoug

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to participate in condensation and cyclization reactions. Commonly employed in medicinal chemistry for modifying indazole-based scaffolds to enhance drug potency and selectivity. Also utilized in the creation of novel psychoactive substances for research purposes, though not approved for human use. Its structural features make it valuable in the design of small molecule therapeutics targeting neurological and inflammatory disorders.

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