3-(4-BROMOPHENYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID

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Reagent Code: #152178
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CAS Number 46413-66-5

science Other reagents with same CAS 46413-66-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 267.08 g/mol
Formula C₁₀H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD06200702
thermostat Physical Properties
Melting Point 258-262 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for designing drugs targeting inflammatory diseases and neurological disorders. Its bromo-functionalized aromatic ring allows for further cross-coupling reactions, enabling the creation of diverse compound libraries in drug discovery. Also employed in research settings to develop new pyrazole-based bioactive molecules with potential antimicrobial and anti-inflammatory properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,540.00
inventory 1g
10-20 days ฿4,090.00
inventory 5g
10-20 days ฿16,480.00

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3-(4-BROMOPHENYL)-1H-PYRAZOLE-5-CARBOXYLIC ACID
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for designing drugs targeting inflammatory diseases and neurological disorders. Its bromo-functionalized aromatic ring allows for further cross-coupling reactions, enabling the creation of diverse compound libraries in drug discovery. Also employed in research settings to develop new pyrazole-based bioactiv

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry for designing drugs targeting inflammatory diseases and neurological disorders. Its bromo-functionalized aromatic ring allows for further cross-coupling reactions, enabling the creation of diverse compound libraries in drug discovery. Also employed in research settings to develop new pyrazole-based bioactive molecules with potential antimicrobial and anti-inflammatory properties.

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