1-(3-Bromophenyl)-1H-Pyrazole-4-Carboxylic Acid

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Reagent Code: #154324
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CAS Number 1156994-32-9

science Other reagents with same CAS 1156994-32-9

blur_circular Chemical Specifications

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Weight 267.08 g/mol
Formula C₁₀H₇BrN₂O₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in medicinal chemistry for constructing pyrazole-based compounds that are explored for their activity in central nervous system disorders and cancer research. Its bromoaryl group allows for further functionalization via cross-coupling reactions, making it valuable in the design of novel drug candidates. Also employed in agrochemical research for developing new active ingredients in crop protection agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,830.00
inventory 250mg
10-20 days ฿6,850.00
inventory 1g
10-20 days ฿18,400.00

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1-(3-Bromophenyl)-1H-Pyrazole-4-Carboxylic Acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in medicinal chemistry for constructing pyrazole-based compounds that are explored for their activity in central nervous system disorders and cancer research. Its bromoaryl group allows for further functionalization via cross-coupling reactions, making it valuable in the design of novel drug candidates.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and analgesic properties. It serves as a building block in medicinal chemistry for constructing pyrazole-based compounds that are explored for their activity in central nervous system disorders and cancer research. Its bromoaryl group allows for further functionalization via cross-coupling reactions, making it valuable in the design of novel drug candidates. Also employed in agrochemical research for developing new active ingredients in crop protection agents.

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