Ethyl 4-Phenylpyrazole-3-carboxylate

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Reagent Code: #182089
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CAS Number 6963-62-8

science Other reagents with same CAS 6963-62-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.24 g/mol
Formula C₁₂H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD01927509
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and COX-2 inhibitors. Its structure supports the creation of bioactive molecules with analgesic and antipyretic properties. Also employed in agrochemical research for designing novel pesticides due to its favorable reactivity and stability in heterocyclic transformations. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,440.00
inventory 250mg
10-20 days ฿5,360.00
inventory 1g
10-20 days ฿13,730.00
inventory 5g
10-20 days ฿49,680.00

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Ethyl 4-Phenylpyrazole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and COX-2 inhibitors. Its structure supports the creation of bioactive molecules with analgesic and antipyretic properties. Also employed in agrochemical research for designing novel pesticides due to its favorable reactivity and stability in heterocyclic transformations. Commonly utilized in medicinal chemistry for scaffold modification and structure-acti

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and COX-2 inhibitors. Its structure supports the creation of bioactive molecules with analgesic and antipyretic properties. Also employed in agrochemical research for designing novel pesticides due to its favorable reactivity and stability in heterocyclic transformations. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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