1-(4-Bromophenyl)-4-methyl-1H-pyrazole

95%

Reagent Code: #152726
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CAS Number 1184673-82-2

science Other reagents with same CAS 1184673-82-2

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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, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the creation of bioactive molecules due to the presence of the pyrazole ring, which is known for its pharmacological activity. Also employed in agrochemical research for designing new pesticides and herbicides, leveraging its stability and reactivity in cross-coupling reactions. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,190.00
inventory 250mg
10-20 days ฿10,360.00
inventory 1g
10-20 days ฿28,580.00

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1-(4-Bromophenyl)-4-methyl-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the creation of bioactive molecules due to the presence of the pyrazole ring, which is known for its pharmacological activity. Also employed in agrochemical research for designing new pesticides and herbicides, leveraging its stability and reactivity in cross-coupling reactions. Commonly utilized in medicin

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of non-steroidal anti-inflammatory drugs (NSAIDs) and selective COX-2 inhibitors. Its structure supports the creation of bioactive molecules due to the presence of the pyrazole ring, which is known for its pharmacological activity. Also employed in agrochemical research for designing new pesticides and herbicides, leveraging its stability and reactivity in cross-coupling reactions. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates.

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