(E)-3-(Dimethylamino)-2-methoxyacrylaldehyde

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Reagent Code: #182441
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CAS Number 13616-34-7

science Other reagents with same CAS 13616-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 129.16 g/mol
Formula C₆H₁₁NO₂
badge Registry Numbers
MDL Number MFCD04973041
thermostat Physical Properties
Boiling Point 304.1°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of fungicides and plant growth regulators. Its α,β-unsaturated aldehyde structure with dimethylamino and methoxy groups enables participation in Michael addition and cyclization reactions, making it valuable in constructing heterocyclic compounds. Commonly employed in the development of strobilurin-class fungicides, which are widely applied in crop protection due to their broad-spectrum activity and low environmental impact. Also utilized in research for designing bioactive molecules with antimicrobial and antifungal properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,350.00
inventory 250mg
10-20 days ฿4,070.00

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(E)-3-(Dimethylamino)-2-methoxyacrylaldehyde
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of fungicides and plant growth regulators. Its α,β-unsaturated aldehyde structure with dimethylamino and methoxy groups enables participation in Michael addition and cyclization reactions, making it valuable in constructing heterocyclic compounds. Commonly employed in the development of strobilurin-class fungicides, which are widely applied in crop protection due to their broad-spectrum activi

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of fungicides and plant growth regulators. Its α,β-unsaturated aldehyde structure with dimethylamino and methoxy groups enables participation in Michael addition and cyclization reactions, making it valuable in constructing heterocyclic compounds. Commonly employed in the development of strobilurin-class fungicides, which are widely applied in crop protection due to their broad-spectrum activity and low environmental impact. Also utilized in research for designing bioactive molecules with antimicrobial and antifungal properties.

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