2,6-Dibromo-p-benzoquinone

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Reagent Code: #180424
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CAS Number 19643-45-9

science Other reagents with same CAS 19643-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.89 g/mol
Formula C₆H₂Br₂O₂
badge Registry Numbers
MDL Number MFCD00016365
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a selective oxidizing agent in organic synthesis, particularly for the oxidation of phenols and hydroquinones to quinones. It is effective in bromination reactions, where it introduces bromine atoms into aromatic compounds under mild conditions. Commonly applied in the preparation of functionalized quinones used in pharmaceuticals, dyes, and electroactive materials. Also serves as a reagent in analytical chemistry for detecting specific functional groups due to its distinct color change during reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,400.00
inventory 250mg
10-20 days ฿14,520.00
inventory 1g
10-20 days ฿39,250.00
inventory 5g
10-20 days ฿141,960.00

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2,6-Dibromo-p-benzoquinone
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Used as a selective oxidizing agent in organic synthesis, particularly for the oxidation of phenols and hydroquinones to quinones. It is effective in bromination reactions, where it introduces bromine atoms into aromatic compounds under mild conditions. Commonly applied in the preparation of functionalized quinones used in pharmaceuticals, dyes, and electroactive materials. Also serves as a reagent in analytical chemistry for detecting specific functional groups due to its distinct color change during re

Used as a selective oxidizing agent in organic synthesis, particularly for the oxidation of phenols and hydroquinones to quinones. It is effective in bromination reactions, where it introduces bromine atoms into aromatic compounds under mild conditions. Commonly applied in the preparation of functionalized quinones used in pharmaceuticals, dyes, and electroactive materials. Also serves as a reagent in analytical chemistry for detecting specific functional groups due to its distinct color change during reactions.

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