1-Chloro-4-(methylsulfonyl)butan-2-one

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Reagent Code: #163817
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CAS Number 2228671-34-7

science Other reagents with same CAS 2228671-34-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.64 g/mol
Formula C₅H₉ClO₃S
badge Registry Numbers
MDL Number MFCD31666473
thermostat Physical Properties
Boiling Point 363.5±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.313±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfone-containing molecules with potential biological activity. Its functional groups enable participation in nucleophilic substitution and condensation reactions, making it valuable in pharmaceutical and agrochemical research. The chloro and ketone functionalities allow for selective modifications, facilitating the construction of complex molecular architectures. It is also employed in the development of specialty chemicals where sulfonyl moieties contribute to solubility, stability, or electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,240.00
inventory 1g
10-20 days ฿4,660.00

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1-Chloro-4-(methylsulfonyl)butan-2-one
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfone-containing molecules with potential biological activity. Its functional groups enable participation in nucleophilic substitution and condensation reactions, making it valuable in pharmaceutical and agrochemical research. The chloro and ketone functionalities allow for selective modifications, facilitating the construction of complex molecular architectures. It is also employed in the development of

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of sulfone-containing molecules with potential biological activity. Its functional groups enable participation in nucleophilic substitution and condensation reactions, making it valuable in pharmaceutical and agrochemical research. The chloro and ketone functionalities allow for selective modifications, facilitating the construction of complex molecular architectures. It is also employed in the development of specialty chemicals where sulfonyl moieties contribute to solubility, stability, or electronic properties.

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