2,3-Dichloro-5,6-dicyano-p-benzoquinone

98%

Reagent Code: #169513
label
Alias Dichlorodicyenobenzenequinone, 2,3-dichloro-5,6-dichlorobenzenequinone, 2,3-dichloro-5,6-dichloro-p-benzenequinone, dichlorodicyenobenzenequinone (DDQ), 2,3-dichloro-5,6-dichlorobenzenequinone
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CAS Number 84-58-2

science Other reagents with same CAS 84-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227 g/mol
Formula C₈Cl₂N₂O₂
badge Registry Numbers
EC Number 201-542-2
MDL Number MFCD00001593
thermostat Physical Properties
Melting Point 210-215 °C (dec.)(lit.)
inventory_2 Storage & Handling
Storage 2~8°C, dry

description Product Description

Widely used as a strong oxidizing agent in organic synthesis, particularly in the conversion of alcohols to carbonyl compounds such as aldehydes and ketones. It is especially effective in dehydrogenation reactions, including the oxidation of dihydroaromatic compounds to their fully aromatic counterparts. Commonly employed in the synthesis of steroids, alkaloids, and other complex molecules where selective and efficient oxidation is required. Also utilized in the preparation of conductive polymers and organic semiconductors due to its electron-accepting properties. Its role in analytical chemistry includes use as a derivatization reagent for detecting compounds with active hydrogens.

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Test Parameter Specification
Melting Point 210-217°C
Purity 98-100
Ash 0.1
Loss on Drying <=0.5
Appearance Yellow to Orange Powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿330.00
inventory 25g
10-20 days ฿790.00
inventory 100g
10-20 days ฿2,500.00
inventory 500g
10-20 days ฿10,000.00
inventory 2.5kg
10-20 days ฿39,110.00
inventory 5kg
10-20 days ฿66,500.00

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2,3-Dichloro-5,6-dicyano-p-benzoquinone
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Widely used as a strong oxidizing agent in organic synthesis, particularly in the conversion of alcohols to carbonyl compounds such as aldehydes and ketones. It is especially effective in dehydrogenation reactions, including the oxidation of dihydroaromatic compounds to their fully aromatic counterparts. Commonly employed in the synthesis of steroids, alkaloids, and other complex molecules where selective and efficient oxidation is required. Also utilized in the preparation of conductive polymers and org

Widely used as a strong oxidizing agent in organic synthesis, particularly in the conversion of alcohols to carbonyl compounds such as aldehydes and ketones. It is especially effective in dehydrogenation reactions, including the oxidation of dihydroaromatic compounds to their fully aromatic counterparts. Commonly employed in the synthesis of steroids, alkaloids, and other complex molecules where selective and efficient oxidation is required. Also utilized in the preparation of conductive polymers and organic semiconductors due to its electron-accepting properties. Its role in analytical chemistry includes use as a derivatization reagent for detecting compounds with active hydrogens.

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