1-Phenyl-1H-pyrazole-3-carbaldehyde

≥95%

Reagent Code: #226325
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CAS Number 40261-59-4

science Other reagents with same CAS 40261-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.18 g/mol
Formula C₁₀H₈N₂O
badge Registry Numbers
MDL Number MFCD08437287
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and antifungal properties. Its aldehyde functional group allows for easy modification, making it valuable in constructing more complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases, which are studied for their pharmacological potential. Also utilized in the preparation of pyrazole-based dyes and fluorescent probes for chemical sensing and imaging applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,020.00
250mg
10-20 days ฿4,310.00
1g
10-20 days ฿13,570.00
5g
10-20 days ฿43,820.00

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1-Phenyl-1H-pyrazole-3-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and antifungal properties. Its aldehyde functional group allows for easy modification, making it valuable in constructing more complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases, which are studied for their pharmacological potential. Also utilized in the preparation of pyrazole-based dy

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with anti-inflammatory, antimicrobial, and antifungal properties. Its aldehyde functional group allows for easy modification, making it valuable in constructing more complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases, which are studied for their pharmacological potential. Also utilized in the preparation of pyrazole-based dyes and fluorescent probes for chemical sensing and imaging applications.

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