N-(5-Chloro-3-((4-(diethylamino)-2-methylphenyl)imino)-4-methyl-6-oxocyclohexa-1,4-dien-1-yl)acetamide

95%

Reagent Code: #220265
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CAS Number 102387-48-4

science Other reagents with same CAS 102387-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.88 g/mol
Formula C₂₀H₂₄ClN₃O₂
badge Registry Numbers
MDL Number MFCD19443390
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of advanced organic dyes and pigments, particularly in the production of high-performance azo dyes for textile and printing industries. Its unique conjugated structure and electron-donating groups enhance color fastness and light stability. Also explored in photovoltaic systems as a sensitizing agent due to its strong absorption in the visible spectrum. Shows potential in pharmaceutical research for developing compounds with biological activity, leveraging its imino and amide functionalities for molecular diversity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,450.00
inventory 1g
10-20 days ฿11,300.00
inventory 5g
10-20 days ฿46,060.00
inventory 250mg
10-20 days ฿4,030.00
N-(5-Chloro-3-((4-(diethylamino)-2-methylphenyl)imino)-4-methyl-6-oxocyclohexa-1,4-dien-1-yl)acetamide
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Used as a key intermediate in the synthesis of advanced organic dyes and pigments, particularly in the production of high-performance azo dyes for textile and printing industries. Its unique conjugated structure and electron-donating groups enhance color fastness and light stability. Also explored in photovoltaic systems as a sensitizing agent due to its strong absorption in the visible spectrum. Shows potential in pharmaceutical research for developing compounds with biological activity, leveraging its

Used as a key intermediate in the synthesis of advanced organic dyes and pigments, particularly in the production of high-performance azo dyes for textile and printing industries. Its unique conjugated structure and electron-donating groups enhance color fastness and light stability. Also explored in photovoltaic systems as a sensitizing agent due to its strong absorption in the visible spectrum. Shows potential in pharmaceutical research for developing compounds with biological activity, leveraging its imino and amide functionalities for molecular diversity.

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