1-p-Tolyl-1H-pyrazole-4-carbaldehyde

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Reagent Code: #242568
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CAS Number 337957-59-2

science Other reagents with same CAS 337957-59-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.21 g/mol
Formula C₁₁H₁₀N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

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 allows for easy functionalization, making it valuable in constructing biologically active molecules. Also employed in agrochemical research for designing new pesticides and herbicides due to its aromatic and heterocyclic properties. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,450.00
inventory 1g
10-20 days ฿8,160.00
inventory 5g
10-20 days ฿32,400.00

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1-p-Tolyl-1H-pyrazole-4-carbaldehyde
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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 allows for easy functionalization, making it valuable in constructing biologically active molecules. Also employed in agrochemical research for designing new pesticides and herbicides due to its aromatic and heterocyclic properties. Commonly utilized in medicinal chemistry for scaffold modification and structure-act

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 allows for easy functionalization, making it valuable in constructing biologically active molecules. Also employed in agrochemical research for designing new pesticides and herbicides due to its aromatic and heterocyclic properties. Commonly utilized in medicinal chemistry for scaffold modification and structure-activity relationship (SAR) studies.

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