Tetrachloro-1,4-benzoquinone

98%, for synthesis

Reagent Code: #128407
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CAS Number 118-75-2

science Other reagents with same CAS 118-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.88 g/mol
Formula C₆Cl₄O₂
badge Registry Numbers
EC Number 204-274-4
MDL Number MFCD00001594
thermostat Physical Properties
Melting Point 295-296 °C(dec.)
inventory_2 Storage & Handling
Density 1.97 g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of quinone-based colorants. It serves as a reagent in organic transformations, including oxidation reactions due to its electron-deficient quinone structure. Employed in research for the development of photoactive compounds and in the preparation of charge-transfer complexes for electronic materials. Also finds use as a catalyst or co-catalyst in certain halogenation processes. Its high reactivity makes it suitable for modifying aromatic systems in pharmaceutical and agrochemical synthesis.

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Test Parameter Specification
Appearance Yellow to Yellow-Green Powder or Crystals
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿1,950.00
inventory 500g
10-20 days ฿5,650.00

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Tetrachloro-1,4-benzoquinone
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Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of quinone-based colorants. It serves as a reagent in organic transformations, including oxidation reactions due to its electron-deficient quinone structure. Employed in research for the development of photoactive compounds and in the preparation of charge-transfer complexes for electronic materials. Also finds use as a catalyst or co-catalyst in certain halogenation processes. Its high reactivity makes it suitable
Used as an intermediate in the synthesis of dyes and pigments, particularly in the production of quinone-based colorants. It serves as a reagent in organic transformations, including oxidation reactions due to its electron-deficient quinone structure. Employed in research for the development of photoactive compounds and in the preparation of charge-transfer complexes for electronic materials. Also finds use as a catalyst or co-catalyst in certain halogenation processes. Its high reactivity makes it suitable for modifying aromatic systems in pharmaceutical and agrochemical synthesis.
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