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

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Reagent Code: #153596
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CAS Number 863752-24-3

science Other reagents with same CAS 863752-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 276.14 g/mol
Formula C₁₂H₁₀BrN₃
badge Registry Numbers
MDL Number MFCD19443341
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of pyrazole-based bioactive compounds. Exhibits utility in agrochemical research for designing novel pesticides and herbicides due to its reactive functional groups. The bromo and nitrile moieties allow for further chemical modifications through cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting anti-inflammatory, antimicrobial, and anticancer agents. Its benzyl and methyl substitutions enhance lipophilicity, improving cell membrane permeability in drug design applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,140.00
inventory 250mg
10-20 days ฿18,230.00
inventory 1g
10-20 days ฿58,830.00

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1-Benzyl-4-bromo-5-methyl-1H-pyrazole-3-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of pyrazole-based bioactive compounds. Exhibits utility in agrochemical research for designing novel pesticides and herbicides due to its reactive functional groups. The bromo and nitrile moieties allow for further chemical modifications through cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relations

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of pyrazole-based bioactive compounds. Exhibits utility in agrochemical research for designing novel pesticides and herbicides due to its reactive functional groups. The bromo and nitrile moieties allow for further chemical modifications through cross-coupling reactions, enabling the construction of complex molecular architectures. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies targeting anti-inflammatory, antimicrobial, and anticancer agents. Its benzyl and methyl substitutions enhance lipophilicity, improving cell membrane permeability in drug design applications.

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