5-methoxy-2-methylbenzaldehyde

≥98%

Reagent Code: #205604
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CAS Number 56724-09-5

science Other reagents with same CAS 56724-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.18 g/mol
Formula C₉H₁₀O₂
badge Registry Numbers
MDL Number MFCD12547802
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain vasodilators and anti-inflammatory agents. It serves as a building block in organic reactions due to the reactivity of the aldehyde group, enabling the formation of Schiff bases, imines, and other derivatives. Also employed in the fragrance industry for imparting floral and fruity notes in perfume formulations. Its methoxy and methyl substituents enhance electron density, making it useful in electrophilic aromatic substitution reactions during fine chemical synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿379.50
inventory 1g
10-20 days ฿2,520.00
inventory 5g
10-20 days ฿11,750.00
5-methoxy-2-methylbenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain vasodilators and anti-inflammatory agents. It serves as a building block in organic reactions due to the reactivity of the aldehyde group, enabling the formation of Schiff bases, imines, and other derivatives. Also employed in the fragrance industry for imparting floral and fruity notes in perfume formulations. Its methoxy and methyl substituents enhance electron density, making it use

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the production of certain vasodilators and anti-inflammatory agents. It serves as a building block in organic reactions due to the reactivity of the aldehyde group, enabling the formation of Schiff bases, imines, and other derivatives. Also employed in the fragrance industry for imparting floral and fruity notes in perfume formulations. Its methoxy and methyl substituents enhance electron density, making it useful in electrophilic aromatic substitution reactions during fine chemical synthesis.

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