4-((Methylsulfonyl)methyl)benzaldehyde

≥95%

Reagent Code: #208675
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CAS Number 156867-56-0

science Other reagents with same CAS 156867-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.24 g/mol
Formula C₉H₁₀O₃S
badge Registry Numbers
MDL Number MFCD21603748
thermostat Physical Properties
Boiling Point 432.5±28.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde functional group allows for easy derivatization, enabling the formation of Schiff bases or other condensation products critical in drug design. Also employed in the preparation of sulfone-containing bioactive molecules due to the electron-withdrawing nature of the sulfonyl group, which can enhance metabolic stability and binding affinity. Additionally, it serves as a building block in agrochemicals and functional materials where aromatic aldehydes with polar substituents are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,930.00
inventory 250mg
10-20 days ฿29,860.00

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4-((Methylsulfonyl)methyl)benzaldehyde
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde functional group allows for easy derivatization, enabling the formation of Schiff bases or other condensation products critical in drug design. Also employed in the preparation of sulfone-containing bioactive molecules due to the electron-withdrawing nature of the sulfonyl group, which can enhance metabolic stability and binding affinity. Additionally,
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its aldehyde functional group allows for easy derivatization, enabling the formation of Schiff bases or other condensation products critical in drug design. Also employed in the preparation of sulfone-containing bioactive molecules due to the electron-withdrawing nature of the sulfonyl group, which can enhance metabolic stability and binding affinity. Additionally, it serves as a building block in agrochemicals and functional materials where aromatic aldehydes with polar substituents are required.
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