1-Ethyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde

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Reagent Code: #184099
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CAS Number 701911-46-8

science Other reagents with same CAS 701911-46-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.1937 g/mol
Formula C₈H₁₂N₂O
badge Registry Numbers
MDL Number MFCD02253752
thermostat Physical Properties
Boiling Point 255 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.06 g/cm3
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients for crop protection products. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of pyrazole-based derivatives with potential antimicrobial, anti-inflammatory, or insecticidal properties. Its aldehyde group enables easy modification through condensation or reduction reactions, facilitating its use in multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,020.00
inventory 5g
10-20 days ฿13,010.00
inventory 10g
10-20 days ฿24,700.00
inventory 250mg
10-20 days ฿1,000.00

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1-Ethyl-3,5-dimethyl-1H-pyrazole-4-carbaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients for crop protection products. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of pyrazole-based derivatives with potential antimicrobial, anti-inflammatory, or insecticidal properties. Its aldehyde group enables easy modification

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of active ingredients for crop protection products. Its structure allows for functionalization in heterocyclic compound design, making it valuable in medicinal chemistry for building bioactive molecules. It is also employed in the preparation of pyrazole-based derivatives with potential antimicrobial, anti-inflammatory, or insecticidal properties. Its aldehyde group enables easy modification through condensation or reduction reactions, facilitating its use in multi-step organic syntheses.

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