1-(5-methylpyridin-2-yl)ethanone

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Reagent Code: #208639
label
Alias 2-acetyl-5-methylpyridine
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CAS Number 5308-63-4

science Other reagents with same CAS 5308-63-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 135.16 g/mol
Formula C₈H₉NO
badge Registry Numbers
MDL Number MFCD06658292
thermostat Physical Properties
Boiling Point 105 °C(Press: 13 Torr)
inventory_2 Storage & Handling
Density 1.036±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active molecules due to the presence of the methylpyridine and ketone functional groups, which allow for further chemical modifications. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates. Also utilized in the production of agrochemicals and functional materials where pyridine derivatives enhance stability and reactivity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,040.00
inventory 5g
10-20 days ฿8,940.00

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1-(5-methylpyridin-2-yl)ethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active molecules due to the presence of the methylpyridine and ketone functional groups, which allow for further chemical modifications. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates. Also utilized in the production of agrochemicals

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active molecules due to the presence of the methylpyridine and ketone functional groups, which allow for further chemical modifications. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates. Also utilized in the production of agrochemicals and functional materials where pyridine derivatives enhance stability and reactivity.

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