3-(4-Methoxyphenyl)-1-phenyl-1H-pyrazole-5-carboxylic acid

≥95%

Reagent Code: #214256
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CAS Number 926257-89-8

science Other reagents with same CAS 926257-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.3 g/mol
Formula C₁₇H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD06337669
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs. Its structure supports activity as a cyclooxygenase (COX) inhibitor, making it valuable in creating non-steroidal anti-inflammatory compounds. Also explored in the design of selective ligands for central nervous system targets due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry research for optimizing drug candidates with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿5,990.00

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3-(4-Methoxyphenyl)-1-phenyl-1H-pyrazole-5-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs. Its structure supports activity as a cyclooxygenase (COX) inhibitor, making it valuable in creating non-steroidal anti-inflammatory compounds. Also explored in the design of selective ligands for central nervous system targets due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry research for optimizing drug candidates with

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and analgesic drugs. Its structure supports activity as a cyclooxygenase (COX) inhibitor, making it valuable in creating non-steroidal anti-inflammatory compounds. Also explored in the design of selective ligands for central nervous system targets due to its ability to cross the blood-brain barrier. Commonly employed in medicinal chemistry research for optimizing drug candidates with improved metabolic stability and binding affinity.

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