4-(Diisopropylamino)benzaldehyde

95%

Reagent Code: #167496
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CAS Number 478682-37-0

science Other reagents with same CAS 478682-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.3 g/mol
Formula C₁₃H₁₉NO
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MDL Number MFCD31391867
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the production of triarylmethane dyes and photochromic compounds. It serves as a building block in organic reactions where aldehyde functionality allows for condensation and nucleophilic addition, enabling the formation of more complex aromatic structures. Its secondary amine group enhances electron-donating properties, making it valuable in the development of sensors and optoelectronic materials. Also employed in research for developing novel amine-responsive reagents and in the preparation of fluorescent probes due to its favorable reactivity and structural characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,440.00
inventory 1g
10-20 days ฿30,870.00
inventory 100mg
10-20 days ฿6,730.00

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4-(Diisopropylamino)benzaldehyde
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Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the production of triarylmethane dyes and photochromic compounds. It serves as a building block in organic reactions where aldehyde functionality allows for condensation and nucleophilic addition, enabling the formation of more complex aromatic structures. Its secondary amine group enhances electron-donating properties, making it valuable in the development of sensors and optoelectronic materials. Also employed in resea

Used as an intermediate in the synthesis of dyes and pharmaceuticals, particularly in the production of triarylmethane dyes and photochromic compounds. It serves as a building block in organic reactions where aldehyde functionality allows for condensation and nucleophilic addition, enabling the formation of more complex aromatic structures. Its secondary amine group enhances electron-donating properties, making it valuable in the development of sensors and optoelectronic materials. Also employed in research for developing novel amine-responsive reagents and in the preparation of fluorescent probes due to its favorable reactivity and structural characteristics.

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