5-Chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde

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Reagent Code: #163678
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CAS Number 318288-78-7

science Other reagents with same CAS 318288-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.626 g/mol
Formula C₁₁H₆ClF₃N₂O
badge Registry Numbers
MDL Number MFCD00793866
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive aldehyde and electron-withdrawing groups, enabling diverse functionalization. Also utilized in the preparation of fluorescent probes and sensors owing to its aromatic and electron-deficient framework.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,460.00
inventory 250mg
10-20 days ฿8,110.00

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5-Chloro-1-phenyl-3-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive aldehyde and electron-withdrawing groups, enabling diverse functionalization. Also utilized in the preparation of flu

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of pyrazole-based bioactive compounds. Its structure supports the creation of derivatives with insecticidal, fungicidal, and anti-inflammatory properties. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the presence of reactive aldehyde and electron-withdrawing groups, enabling diverse functionalization. Also utilized in the preparation of fluorescent probes and sensors owing to its aromatic and electron-deficient framework.

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