2-Bromo-6-fluorothioanisole

95%

Reagent Code: #155041
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CAS Number 1370025-53-8

science Other reagents with same CAS 1370025-53-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.1 g/mol
Formula C₇H₆BrFS
badge Registry Numbers
MDL Number MFCD22056775
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its bromo and fluoro substituents allow selective cross-coupling reactions, while the thioanisole group acts as a directing group to control the regioselectivity of chemical reactions. This makes it valuable in building complex molecules via palladium- or copper-catalyzed reactions, such as Suzuki or Ullmann coupling. Commonly employed in research settings for constructing bioactive molecules, including antimicrobials, and functionalized aromatic systems.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,800.00
250mg
10-20 days ฿3,040.00
1g
10-20 days ฿6,070.00
5g
10-20 days ฿23,130.00
10g
10-20 days ฿32,550.00

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2-Bromo-6-fluorothioanisole
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its bromo and fluoro substituents allow selective cross-coupling reactions, while the thioanisole group acts as a directing group to control the regioselectivity of chemical reactions. This makes it valuable in building complex molecules via palladium- or copper-catalyzed reactions, such as Suzuki or Ullmann coupling. Commonly employed in research settings for c

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its bromo and fluoro substituents allow selective cross-coupling reactions, while the thioanisole group acts as a directing group to control the regioselectivity of chemical reactions. This makes it valuable in building complex molecules via palladium- or copper-catalyzed reactions, such as Suzuki or Ullmann coupling. Commonly employed in research settings for constructing bioactive molecules, including antimicrobials, and functionalized aromatic systems.

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