(2-Bromoethyl)(4-fluorophenyl)sulfane

95%

Reagent Code: #141371
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CAS Number 339363-85-8

science Other reagents with same CAS 339363-85-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.12 g/mol
Formula C₈H₈FSBr
badge Registry Numbers
MDL Number MFCD09944899
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of biologically active molecules, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in constructing sulfur-containing aromatic systems. The presence of both bromo and fluoro groups enables sequential cross-coupling reactions, useful in developing complex drug candidates. It is also employed in the synthesis of thioether derivatives with potential antimicrobial or anti-inflammatory properties. Due to its reactivity, it is handled under controlled conditions for safe use in laboratory-scale transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,210.00
inventory 250mg
10-20 days ฿13,930.00
inventory 1g
10-20 days ฿37,600.00

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(2-Bromoethyl)(4-fluorophenyl)sulfane
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of biologically active molecules, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in constructing sulfur-containing aromatic systems. The presence of both bromo and fluoro groups enables sequential cross-coupling reactions, useful in developing complex drug candidates. It is also employed in the synthesis of thioether derivatives with potential

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of biologically active molecules, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in constructing sulfur-containing aromatic systems. The presence of both bromo and fluoro groups enables sequential cross-coupling reactions, useful in developing complex drug candidates. It is also employed in the synthesis of thioether derivatives with potential antimicrobial or anti-inflammatory properties. Due to its reactivity, it is handled under controlled conditions for safe use in laboratory-scale transformations.

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