1-Methylthio-2-propanone

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Reagent Code: #213317
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CAS Number 14109-72-9

science Other reagents with same CAS 14109-72-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 104.17 g/mol
Formula C₄H₈OS
badge Registry Numbers
MDL Number MFCD00015325
thermostat Physical Properties
Boiling Point 69-70 °C at 30 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfur-containing compounds due to the thioether functional group. Commonly employed in the development of crop protection agents and active ingredients in pesticides. Also utilized in the synthesis of certain flavor and fragrance compounds, where sulfur functionalities contribute to aroma profiles. Its reactivity allows for easy modification in multi-step synthetic routes, making it valuable in research and industrial chemistry.

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inventory 25g
10-20 days ฿29,440.00

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1-Methylthio-2-propanone
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Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfur-containing compounds due to the thioether functional group. Commonly employed in the development of crop protection agents and active ingredients in pesticides. Also utilized in the synthesis of certain flavor and fragrance compounds, where sulfur functionalities contribute to aroma profiles. Its reactivity allows for easy modification in mult

Used primarily as an intermediate in organic synthesis, especially in the production of pharmaceuticals and agrochemicals. It serves as a building block for sulfur-containing compounds due to the thioether functional group. Commonly employed in the development of crop protection agents and active ingredients in pesticides. Also utilized in the synthesis of certain flavor and fragrance compounds, where sulfur functionalities contribute to aroma profiles. Its reactivity allows for easy modification in multi-step synthetic routes, making it valuable in research and industrial chemistry.

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