4-Bromo-1-(4-isopropylphenyl)-1H-pyrazole

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Reagent Code: #155077
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CAS Number 1784189-46-3

science Other reagents with same CAS 1784189-46-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.15 g/mol
Formula C₁₂H₁₃BrN₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and cannabinoid receptor modulators. Its structural features allow for selective derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in agrochemical research for designing bioactive molecules with pesticidal or fungicidal activity. Commonly utilized in Suzuki and other cross-coupling reactions to build complex aromatic systems in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,760.00
inventory 250mg
10-20 days ฿12,980.00
inventory 1g
10-20 days ฿35,300.00

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4-Bromo-1-(4-isopropylphenyl)-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and cannabinoid receptor modulators. Its structural features allow for selective derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in agrochemical research for designing bioactive molecules with pesticidal or fungicidal activity. Commonly utilized in Suzuki and other cross-coupling reacti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs) and cannabinoid receptor modulators. Its structural features allow for selective derivatization, making it valuable in medicinal chemistry for optimizing drug potency and metabolic stability. Also employed in agrochemical research for designing bioactive molecules with pesticidal or fungicidal activity. Commonly utilized in Suzuki and other cross-coupling reactions to build complex aromatic systems in drug discovery programs.

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