Ethyl 1-methyl-1H-indazole-3-carboxylate

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Reagent Code: #83115
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CAS Number 220488-05-1

science Other reagents with same CAS 220488-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.23 g/mol
Formula C₁₁H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD07368499
thermostat Physical Properties
Melting Point 58 °C
Boiling Point 326.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

Ethyl 1-methyl-1H-indazole-3-carboxylate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting central nervous system disorders. Its indazole core structure is often incorporated into molecules designed to interact with specific receptors or enzymes, making it valuable in the creation of potential therapeutic agents. Additionally, this compound is explored in medicinal chemistry for its role in developing inhibitors or modulators of protein-protein interactions, which are crucial in treating diseases like cancer and inflammation. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,000.00
inventory 250mg
10-20 days ฿17,280.00
inventory 1g
10-20 days ฿43,200.00

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Ethyl 1-methyl-1H-indazole-3-carboxylate
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Ethyl 1-methyl-1H-indazole-3-carboxylate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting central nervous system disorders. Its indazole core structure is often incorporated into molecules designed to interact with specific receptors or enzymes, making it valuable in the creation of potential therapeutic agents. Additionally, this compound is explored in medicinal chemistry for its role in developing inhibitors or modulators of protein-protein interactions, which are crucial in treating diseases like cancer and inflammation. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.
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