3-Bromo-4-methyl-1-phenyl-1H-pyrazole

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Reagent Code: #117989
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CAS Number 1700661-39-7

science Other reagents with same CAS 1700661-39-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.10 g/mol
Formula C₁₀H₉BrN₂
badge Registry Numbers
MDL Number MFCD28247151
thermostat Physical Properties
Boiling Point 319.1±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both a bromine atom and a phenyl group, makes it particularly useful in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in the preparation of heterocyclic compounds, which are often explored for their biological activities, including potential use in drug discovery and development. The presence of the pyrazole ring further enhances its utility in designing compounds with specific target interactions, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿26,280.00
inventory 100mg
10-20 days ฿13,149.00

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3-Bromo-4-methyl-1-phenyl-1H-pyrazole
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both a bromine atom and a phenyl group, makes it particularly useful in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, which are essential in the synthesis of pharmaceuticals and agrochemicals. Additionally, it is employed in the preparation of heterocyclic compounds, which are often explored for their biological activities, including potential use in drug discovery and development. The presence of the pyrazole ring further enhances its utility in designing compounds with specific target interactions, making it valuable in medicinal chemistry research.
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