4-Hydroxy-3,5-dimethoxybenzaldehyde azine

99%

Reagent Code: #195945
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CAS Number 14414-32-5

science Other reagents with same CAS 14414-32-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.36 g/mol
Formula C₁₈H₂₀N₂O₆
badge Registry Numbers
MDL Number MFCD00008363
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of lignans and other bioactive natural products, this compound plays an important role in pharmaceutical research, particularly in the development of anticancer and antioxidant agents. Its structure allows for selective functionalization, making it valuable in creating analogs for structure-activity relationship studies. Additionally, it serves as a building block in the preparation of chiral ligands and catalysts used in asymmetric synthesis. Due to its stability and reactivity profile, it is also employed in the development of sensors and functional materials where aromatic aldehyde derivatives are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿3,140.00
inventory 5g
10-20 days ฿8,680.00
inventory 25g
10-20 days ฿28,400.00
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4-Hydroxy-3,5-dimethoxybenzaldehyde azine
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Used as a key intermediate in the synthesis of lignans and other bioactive natural products, this compound plays an important role in pharmaceutical research, particularly in the development of anticancer and antioxidant agents. Its structure allows for selective functionalization, making it valuable in creating analogs for structure-activity relationship studies. Additionally, it serves as a building block in the preparation of chiral ligands and catalysts used in asymmetric synthesis. Due to its stabil

Used as a key intermediate in the synthesis of lignans and other bioactive natural products, this compound plays an important role in pharmaceutical research, particularly in the development of anticancer and antioxidant agents. Its structure allows for selective functionalization, making it valuable in creating analogs for structure-activity relationship studies. Additionally, it serves as a building block in the preparation of chiral ligands and catalysts used in asymmetric synthesis. Due to its stability and reactivity profile, it is also employed in the development of sensors and functional materials where aromatic aldehyde derivatives are required.

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