4-Bromo-1-(3-(trifluoromethyl)phenyl)-1H-pyrazole

96%

Reagent Code: #152800
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CAS Number 1353855-69-2

science Other reagents with same CAS 1353855-69-2

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inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, and insecticidal properties. Its structure supports the construction of pyrazole-based compounds that are prevalent in modern drug design due to their metabolic stability and favorable interactions with biological targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds. Also utilized in the preparation of novel trifluoromethylated aromatic systems to enhance lipophilicity and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,040.00
inventory 250mg
10-20 days ฿2,470.00

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4-Bromo-1-(3-(trifluoromethyl)phenyl)-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, and insecticidal properties. Its structure supports the construction of pyrazole-based compounds that are prevalent in modern drug design due to their metabolic stability and favorable interactions with biological targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compo

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, and insecticidal properties. Its structure supports the construction of pyrazole-based compounds that are prevalent in modern drug design due to their metabolic stability and favorable interactions with biological targets. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize lead compounds. Also utilized in the preparation of novel trifluoromethylated aromatic systems to enhance lipophilicity and bioavailability in drug candidates.

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