Ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate

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Reagent Code: #184889
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CAS Number 98475-71-9

science Other reagents with same CAS 98475-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.14 g/mol
Formula C₁₃H₁₀BrN₃O₂
badge Registry Numbers
MDL Number MFCD17215110
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure supports the construction of pyrazole-based bioactive molecules, which are prevalent in drug discovery due to their enzyme inhibitory properties. Commonly employed in research settings for generating analogs in structure-activity relationship (SAR) studies. Also utilized in agrochemical research for developing new pesticidal and fungicidal agents owing to its electron-withdrawing cyano and bromo substituents that enhance biological activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,020.00
inventory 1g
10-20 days ฿30,060.00
inventory 100mg
10-20 days ฿4,620.00

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Ethyl 1-(4-bromophenyl)-5-cyano-1H-pyrazole-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure supports the construction of pyrazole-based bioactive molecules, which are prevalent in drug discovery due to their enzyme inhibitory properties. Commonly employed in research settings for generating analogs in structure-activity relationship (SAR) studies. Also utilized in agrochemical research for developing new pesticidal and fungicidal agen

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and anticancer compounds. Its structure supports the construction of pyrazole-based bioactive molecules, which are prevalent in drug discovery due to their enzyme inhibitory properties. Commonly employed in research settings for generating analogs in structure-activity relationship (SAR) studies. Also utilized in agrochemical research for developing new pesticidal and fungicidal agents owing to its electron-withdrawing cyano and bromo substituents that enhance biological activity.

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