3-((6-Methylpyridin-2-yl)ethynyl)cyclohex-2-en-1-one O-methyl oxime

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Reagent Code: #221182
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CAS Number 924298-51-1

science Other reagents with same CAS 924298-51-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.3 g/mol
Formula C₁₅H₁₆N₂O
badge Registry Numbers
MDL Number MFCD17018722
thermostat Physical Properties
Boiling Point 361.4±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.03±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure enables selective binding to protein targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its metabolic stability and ability to enhance potency. Also utilized in research settings for creating analogs in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,190.00
inventory 10mg
10-20 days ฿18,490.00
inventory 25mg
10-20 days ฿36,940.00

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3-((6-Methylpyridin-2-yl)ethynyl)cyclohex-2-en-1-one O-methyl oxime
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure enables selective binding to protein targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its metabolic stability and ability to enhance potency. Also utilized in research settings for creating analogs in structure-activity relationship (SAR) studies.

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure enables selective binding to protein targets involved in cell signaling pathways. Commonly employed in medicinal chemistry for optimizing drug candidates due to its metabolic stability and ability to enhance potency. Also utilized in research settings for creating analogs in structure-activity relationship (SAR) studies.

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