5-(dimethylamino)-2-nitrobenzaldehyde

95%

Reagent Code: #177293
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CAS Number 548798-23-8

science Other reagents with same CAS 548798-23-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 194.19 g/mol
Formula C₉H₁₀N₂O₃
badge Registry Numbers
MDL Number MFCD05148755
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-donating and light-absorbing properties. Commonly employed in the development of sensors for detecting metal ions and pH changes in solution, thanks to its distinct color shift upon protonation or coordination. Also utilized in organic synthesis for constructing heterocyclic compounds, particularly in the preparation of amino-substituted aromatic systems through reductive amination or condensation reactions. Its aldehyde group allows for easy functionalization in Schiff base formation, making it valuable in coordination chemistry and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,290.00
inventory 250mg
10-20 days ฿7,810.00

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5-(dimethylamino)-2-nitrobenzaldehyde
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Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-donating and light-absorbing properties. Commonly employed in the development of sensors for detecting metal ions and pH changes in solution, thanks to its distinct color shift upon protonation or coordination. Also utilized in organic synthesis for constructing heterocyclic compounds, particularly in the preparation of amino-substituted aromatic systems through reductive amination or conden

Used as a key intermediate in the synthesis of fluorescent dyes and optical brighteners due to its strong electron-donating and light-absorbing properties. Commonly employed in the development of sensors for detecting metal ions and pH changes in solution, thanks to its distinct color shift upon protonation or coordination. Also utilized in organic synthesis for constructing heterocyclic compounds, particularly in the preparation of amino-substituted aromatic systems through reductive amination or condensation reactions. Its aldehyde group allows for easy functionalization in Schiff base formation, making it valuable in coordination chemistry and medicinal chemistry research.

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