(3-Trifluoromethyl-1H-pyrazol-4-yl)methanol

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Reagent Code: #240871
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CAS Number 1001020-13-8

science Other reagents with same CAS 1001020-13-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.1 g/mol
Formula C₅H₅F₃N₂O
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of pyrazole-based compounds known for insecticidal, fungicidal, and herbicidal activities. Also employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents due to the stability and polarity imparted by the trifluoromethyl group. The hydroxyl functionality allows further derivatization, making it valuable in building complex molecules for drug discovery and crop protection products.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿520.00
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿4,800.00

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(3-Trifluoromethyl-1H-pyrazol-4-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of pyrazole-based compounds known for insecticidal, fungicidal, and herbicidal activities. Also employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents due to the stability and polarity imparted by the trifluoromethyl group. The hydroxyl functionality allows further derivatization, making it valua

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive molecules. Its structure supports the creation of pyrazole-based compounds known for insecticidal, fungicidal, and herbicidal activities. Also employed in medicinal chemistry for designing kinase inhibitors and anti-inflammatory agents due to the stability and polarity imparted by the trifluoromethyl group. The hydroxyl functionality allows further derivatization, making it valuable in building complex molecules for drug discovery and crop protection products.

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