4-Ethynyl-1-methyl-1H-pyrazole

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Reagent Code: #183996
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CAS Number 39806-89-8

science Other reagents with same CAS 39806-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 106.13 g/mol
Formula C₆H₆N₂
badge Registry Numbers
MDL Number MFCD17281917
inventory_2 Storage & Handling
Storage Dry, 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its alkyne functionality allows for efficient coupling reactions, such as click chemistry, enabling rapid assembly of complex molecules in drug discovery. Also employed in agrochemical research to design novel pesticides with improved selectivity and potency. Its structural features enhance binding affinity in targeted biological pathways, making it valuable in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,080.00
inventory 250mg
10-20 days ฿2,440.00
inventory 500mg
10-20 days ฿4,080.00
inventory 1g
10-20 days ฿7,300.00

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4-Ethynyl-1-methyl-1H-pyrazole
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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 alkyne functionality allows for efficient coupling reactions, such as click chemistry, enabling rapid assembly of complex molecules in drug discovery. Also employed in agrochemical research to design novel pesticides with improved selectivity and potency. Its structural features enhance binding affinity in targeted biological pathways, making it valuable in medici

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its alkyne functionality allows for efficient coupling reactions, such as click chemistry, enabling rapid assembly of complex molecules in drug discovery. Also employed in agrochemical research to design novel pesticides with improved selectivity and potency. Its structural features enhance binding affinity in targeted biological pathways, making it valuable in medicinal chemistry.

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