1-Bromo-2,5-difluoro-4-hydroxybenzene

95%

Reagent Code: #152635
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CAS Number 486424-36-6

science Other reagents with same CAS 486424-36-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.99 g/mol
Formula C₆H₃BrF₂O
badge Registry Numbers
MDL Number MFCD04973751
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure allows for selective functionalization, making it valuable in building complex molecules where fluorine substitution enhances biological activity or metabolic stability. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the difluorophenol moiety into target compounds. Also utilized in the preparation of liquid crystals and functional materials requiring specific electronic or steric properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿470.00
inventory 1g
10-20 days ฿1,200.00
inventory 5g
10-20 days ฿2,560.00
inventory 10g
10-20 days ฿4,560.00
inventory 25g
10-20 days ฿9,190.00
inventory 100g
10-20 days ฿31,520.00

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1-Bromo-2,5-difluoro-4-hydroxybenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure allows for selective functionalization, making it valuable in building complex molecules where fluorine substitution enhances biological activity or metabolic stability. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the difluorophenol moiety into target compounds. Also utilized in the preparation of liqui

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure allows for selective functionalization, making it valuable in building complex molecules where fluorine substitution enhances biological activity or metabolic stability. Commonly employed in cross-coupling reactions and nucleophilic substitutions to introduce the difluorophenol moiety into target compounds. Also utilized in the preparation of liquid crystals and functional materials requiring specific electronic or steric properties.

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