ethyl 3-acetamido-5-bromo-1-methyl-1H-pyrazole-4-carboxylate

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Reagent Code: #196531
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CAS Number 1017802-89-9

science Other reagents with same CAS 1017802-89-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.11 g/mol
Formula C₉H₁₂BrN₃O₃
badge Registry Numbers
MDL Number MFCD28955023
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure allows for selective modification, making it valuable in medicinal chemistry for designing bioactive molecules. Commonly employed in research settings to construct pyrazole-based scaffolds that exhibit potential therapeutic activity. Also utilized in agrochemical research for developing novel pesticides due to its reactivity and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿33,400.00

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ethyl 3-acetamido-5-bromo-1-methyl-1H-pyrazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure allows for selective modification, making it valuable in medicinal chemistry for designing bioactive molecules. Commonly employed in research settings to construct pyrazole-based scaffolds that exhibit potential therapeutic activity. Also utilized in agrochemical research for developing novel pesticides due to its reactivity and function

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure allows for selective modification, making it valuable in medicinal chemistry for designing bioactive molecules. Commonly employed in research settings to construct pyrazole-based scaffolds that exhibit potential therapeutic activity. Also utilized in agrochemical research for developing novel pesticides due to its reactivity and functional group compatibility.

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