4-(4-Bromophenyl)-1-methylpyrazol-5-amine

95%

Reagent Code: #150412
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CAS Number 1248796-80-6

science Other reagents with same CAS 1248796-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.11 g/mol
Formula C₁₀H₁₀BrN₃
badge Registry Numbers
MDL Number MFCD14657245
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and functional materials where substituted pyrazoles are required. Its bromo functionality allows for further cross-coupling reactions, enabling structural diversification in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,120.00
inventory 250mg
10-20 days ฿6,190.00
inventory 1g
10-20 days ฿18,240.00

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4-(4-Bromophenyl)-1-methylpyrazol-5-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and functional materials where substituted pyrazoles are required. Its bromo functionality allows for further cross-coupling reactions, enabling

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to target proteins. Also utilized in the preparation of agrochemicals and functional materials where substituted pyrazoles are required. Its bromo functionality allows for further cross-coupling reactions, enabling structural diversification in drug discovery programs.

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