4-(1H-Pyrazol-1-yl)benzaldehyde

99.9%

Reagent Code: #195910
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CAS Number 99662-34-7

science Other reagents with same CAS 99662-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₁₀H₈N₂O
badge Registry Numbers
MDL Number MFCD02681938
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in cross-coupling reactions and heterocyclic synthesis to create compounds with potential anti-inflammatory, anticancer, or antimicrobial activity. Also utilized in materials science for the preparation of organic semiconductors and fluorescent dyes due to its conjugated aromatic system.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿750.00
inventory 5g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿9,600.00
inventory 10g
10-20 days ฿3,980.00

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4-(1H-Pyrazol-1-yl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in cross-coupling reactions and heterocyclic synthesis to create compounds with potential anti-inflammatory, anticancer, or antimicrobial activity. Also utilized in materials science for

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building more complex molecules. Commonly employed in cross-coupling reactions and heterocyclic synthesis to create compounds with potential anti-inflammatory, anticancer, or antimicrobial activity. Also utilized in materials science for the preparation of organic semiconductors and fluorescent dyes due to its conjugated aromatic system.

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