4-(DIOCTYLAMINO)-4'-(TRIFLUOROACETYL) AZ

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Reagent Code: #167902
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CAS Number 193154-07-3

science Other reagents with same CAS 193154-07-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 517.6692 g/mol
Formula C₃₀H₄₂F₃N₃O
badge Registry Numbers
MDL Number MFCD05865255
thermostat Physical Properties
Boiling Point 594.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.06±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of advanced organic materials, particularly in the development of nonlinear optical (NLO) compounds. Its structure supports charge transfer properties, making it valuable in designing electro-optic devices and photonic technologies. The presence of trifluoroacetyl and dialkylamino groups enhances its polarity and stability, which is beneficial for applications in organic semiconductors and laser-responsive materials. Also explored in research for fluorescent probes due to its electron-donating and electron-accepting moieties, enabling use in sensors and imaging agents.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿32,000.00
inventory 100mg
10-20 days ฿64,000.00

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4-(DIOCTYLAMINO)-4'-(TRIFLUOROACETYL) AZ
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Used as an intermediate in the synthesis of advanced organic materials, particularly in the development of nonlinear optical (NLO) compounds. Its structure supports charge transfer properties, making it valuable in designing electro-optic devices and photonic technologies. The presence of trifluoroacetyl and dialkylamino groups enhances its polarity and stability, which is beneficial for applications in organic semiconductors and laser-responsive materials. Also explored in research for fluorescent probes d
Used as an intermediate in the synthesis of advanced organic materials, particularly in the development of nonlinear optical (NLO) compounds. Its structure supports charge transfer properties, making it valuable in designing electro-optic devices and photonic technologies. The presence of trifluoroacetyl and dialkylamino groups enhances its polarity and stability, which is beneficial for applications in organic semiconductors and laser-responsive materials. Also explored in research for fluorescent probes due to its electron-donating and electron-accepting moieties, enabling use in sensors and imaging agents.
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