3-Phenyl-1H-pyrazole-4-carboxaldehyde

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Reagent Code: #224828
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CAS Number 26033-20-5

science Other reagents with same CAS 26033-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₁₀H₈N₂O
badge Registry Numbers
MDL Number MFCD00216971
thermostat Physical Properties
Melting Point 146-148 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of pyrazole-based compounds with biological activity, including potential anticancer and antimicrobial drugs. Its aldehyde functional group allows for easy modification through condensation or reduction reactions, enabling the creation of diverse derivatives for structure-activity relationship studies in medicinal chemistry. Also employed in agrochemical research for designing new crop protection agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿550.00
inventory 5g
10-20 days ฿1,580.00
inventory 10g
10-20 days ฿3,100.00
inventory 25g
10-20 days ฿7,670.00
inventory 100g
10-20 days ฿20,610.00

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3-Phenyl-1H-pyrazole-4-carboxaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of pyrazole-based compounds with biological activity, including potential anticancer and antimicrobial drugs. Its aldehyde functional group allows for easy modification through condensation or reduction reactions, enabling the creation of diverse derivatives for structure-activity relationship studies in medicin

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and anti-inflammatory agents. It serves as a building block in the preparation of pyrazole-based compounds with biological activity, including potential anticancer and antimicrobial drugs. Its aldehyde functional group allows for easy modification through condensation or reduction reactions, enabling the creation of diverse derivatives for structure-activity relationship studies in medicinal chemistry. Also employed in agrochemical research for designing new crop protection agents.

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