1,4-Dimethyl-1H-Pyrazole-5-Carbaldehyde

98%

Reagent Code: #179110
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CAS Number 1171645-70-7

science Other reagents with same CAS 1171645-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.14 g/mol
Formula C₆H₈N₂O
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies. Also employed in agrochemical research for designing novel pesticides and herbicides due to the bioactivity associated with pyrazole scaffolds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,900.00
inventory 250mg
10-20 days ฿6,190.00
inventory 5g
10-20 days ฿51,300.00
inventory 10g
10-20 days ฿79,230.00
inventory 1g
10-20 days ฿13,940.00

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1,4-Dimethyl-1H-Pyrazole-5-Carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for structure-activity relationshi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with anti-inflammatory and analgesic properties. It serves as a building block in heterocyclic chemistry, enabling the construction of complex pyrazole derivatives. Its aldehyde functional group allows for easy modification through condensation, reduction, or nucleophilic addition reactions, making it valuable in medicinal chemistry for structure-activity relationship (SAR) studies. Also employed in agrochemical research for designing novel pesticides and herbicides due to the bioactivity associated with pyrazole scaffolds.

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