1-(4-Bromophenyl)-3-methyl-1H-pyrazol-5-amine

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Reagent Code: #151031
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CAS Number 82447-61-8

science Other reagents with same CAS 82447-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.11 g/mol
Formula C₁₀H₁₀BrN₃
badge Registry Numbers
MDL Number MFCD03848265
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and antimicrobial properties. It serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives that are of interest in medicinal research. Its bromo and amino functional groups allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions, making it valuable in drug discovery and the design of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,640.00
inventory 250mg
10-20 days ฿4,800.00
inventory 1g
10-20 days ฿9,600.00

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1-(4-Bromophenyl)-3-methyl-1H-pyrazol-5-amine
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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 antimicrobial properties. It serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives that are of interest in medicinal research. Its bromo and amino functional groups allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions, making it valuable in

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules with potential anti-inflammatory and antimicrobial properties. It serves as a building block in heterocyclic chemistry, enabling the construction of more complex pyrazole derivatives that are of interest in medicinal research. Its bromo and amino functional groups allow for further chemical modifications through cross-coupling reactions and nucleophilic substitutions, making it valuable in drug discovery and the design of new therapeutic agents.

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