1-(Chloromethyl)-4-(methylsulfonyl)benzene

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Reagent Code: #156900
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CAS Number 40517-43-9

science Other reagents with same CAS 40517-43-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.67 g/mol
Formula C₈H₉O₂SCl
badge Registry Numbers
MDL Number MFCD00079774
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. Its chloromethyl group readily undergoes nucleophilic substitution, enabling the introduction of the 4-(methylsulfonyl)benzyl moiety into target molecules. It is particularly valuable in the synthesis of sulfone-containing bioactive compounds. Additionally, it can act as a building block in the development of functional materials and specialty chemicals where sulfonyl groups impart desired polarity or stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿980.00
inventory 5g
10-20 days ฿2,980.00
inventory 25g
10-20 days ฿9,470.00

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1-(Chloromethyl)-4-(methylsulfonyl)benzene
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. Its chloromethyl group readily undergoes nucleophilic substitution, enabling the introduction of the 4-(methylsulfonyl)benzyl moiety into target molecules. It is particularly valuable in the synthesis of sulfone-containing bioactive compounds. Additionally, it can act as a building block in the development of functional materials and specialty chemicals where sulfonyl grou

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and agrochemicals. Its chloromethyl group readily undergoes nucleophilic substitution, enabling the introduction of the 4-(methylsulfonyl)benzyl moiety into target molecules. It is particularly valuable in the synthesis of sulfone-containing bioactive compounds. Additionally, it can act as a building block in the development of functional materials and specialty chemicals where sulfonyl groups impart desired polarity or stability.

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