2-(4-Bromo-1H-pyrazol-1-yl)-2-methylpropanenitrile

95%

Reagent Code: #150751
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CAS Number 2088840-42-8

science Other reagents with same CAS 2088840-42-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.06 g/mol
Formula C₇H₈BrN₃
badge Registry Numbers
MDL Number MFCD30145512
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Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of biologically active compounds by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromo functional group, which allows further cross-coupling reactions such as Suzuki or Heck reactions. 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 ฿10,890.00
inventory 250mg
10-20 days ฿21,790.00
inventory 1g
10-20 days ฿58,990.00

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2-(4-Bromo-1H-pyrazol-1-yl)-2-methylpropanenitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of biologically active compounds by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromo functional group, which allows further cross-coupling reactions such as Suzuki or Heck reactions. Also utilized in agrochemical resear

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the formation of biologically active compounds by serving as a building block in heterocyclic chemistry. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the bromo functional group, which allows further cross-coupling reactions such as Suzuki or Heck reactions. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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