Ethyl 5-amino-1-phenyl-1H-pyrazole-3-carboxylate

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Reagent Code: #182087
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CAS Number 866837-96-9

science Other reagents with same CAS 866837-96-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.25 g/mol
Formula C₁₂H₁₃N₃O₂
badge Registry Numbers
MDL Number MFCD07388406
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the construction of pyrazole-based bioactive molecules, which are known for their analgesic, antipyretic, and anti-cancer properties. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel pesticides and herbicides 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 ฿1,050.00
inventory 250mg
10-20 days ฿1,500.00
inventory 1g
10-20 days ฿4,850.00
inventory 5g
10-20 days ฿12,780.00

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Ethyl 5-amino-1-phenyl-1H-pyrazole-3-carboxylate
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Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the construction of pyrazole-based bioactive molecules, which are known for their analgesic, antipyretic, and anti-cancer properties. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel

Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the construction of pyrazole-based bioactive molecules, which are known for their analgesic, antipyretic, and anti-cancer properties. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its favorable reactivity and stability in multi-step organic transformations.

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