1-Benzyl-4-bromo-3-methyl-1H-pyrazole-5-carbonitrile

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Reagent Code: #152388
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CAS Number 1352925-64-4

science Other reagents with same CAS 1352925-64-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.13 g/mol
Formula C₁₂H₁₀BrN₃
badge Registry Numbers
MDL Number MFCD19443346
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the construction of bioactive molecules due to the presence of reactive bromo and nitrile groups, enabling cross-coupling reactions and functional group transformations. Commonly employed in medicinal chemistry for scaffold modification in drug discovery programs targeting cancer and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,940.00
inventory 250mg
10-20 days ฿16,660.00
inventory 1g
10-20 days ฿50,430.00

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1-Benzyl-4-bromo-3-methyl-1H-pyrazole-5-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the construction of bioactive molecules due to the presence of reactive bromo and nitrile groups, enabling cross-coupling reactions and functional group transformations. Commonly employed in medicinal chemistry for scaffold modification in drug discovery programs targeting cancer and central nervous system disorders. Also utiliz

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and anti-inflammatory compounds. Its structure supports the construction of bioactive molecules due to the presence of reactive bromo and nitrile groups, enabling cross-coupling reactions and functional group transformations. Commonly employed in medicinal chemistry for scaffold modification in drug discovery programs targeting cancer and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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