(E)-3-(Dimethylamino)-1-(pyridin-4-yl)prop-2-en-1-one

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Reagent Code: #184256
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CAS Number 123367-27-1

science Other reagents with same CAS 123367-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 176.2 g/mol
Formula C₁₀H₁₂N₂O
badge Registry Numbers
MDL Number MFCD00115179
thermostat Physical Properties
Melting Point 114℃ (ethyl acetate isopropyl ether )
Boiling Point 281.4±36.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.070±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports conjugation in organic frameworks, making it valuable in creating biologically active molecules. Also employed in research for developing fluorescent probes due to its ability to undergo intramolecular charge transfer. Commonly utilized in medicinal chemistry for building heterocyclic compounds with potential anti-inflammatory and antimicrobial properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,530.00
inventory 5g
10-20 days ฿9,680.00
inventory 250mg
10-20 days ฿2,600.00

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(E)-3-(Dimethylamino)-1-(pyridin-4-yl)prop-2-en-1-one
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports conjugation in organic frameworks, making it valuable in creating biologically active molecules. Also employed in research for developing fluorescent probes due to its ability to undergo intramolecular charge transfer. Commonly utilized in medicinal chemistry for building heterocyclic compounds with potential anti-inflammatory and antimicrobial

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports conjugation in organic frameworks, making it valuable in creating biologically active molecules. Also employed in research for developing fluorescent probes due to its ability to undergo intramolecular charge transfer. Commonly utilized in medicinal chemistry for building heterocyclic compounds with potential anti-inflammatory and antimicrobial properties.

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