2,5-Dimethoxybenzene-1,4-diol

95%

Reagent Code: #129986
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CAS Number 13239-13-9

science Other reagents with same CAS 13239-13-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.16 g/mol
Formula C₈H₁₀O₄
badge Registry Numbers
MDL Number MFCD24713419
thermostat Physical Properties
Melting Point 170 °C
Boiling Point 355.4±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.267±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pharmaceuticals. It serves as a building block in the development of antioxidants due to its phenolic structure, which can scavenge free radicals. Also employed in research settings for the synthesis of substituted quinones, which have applications in materials science and bioactive compound development. Its electron-rich aromatic system makes it useful in the study of charge-transfer complexes and electroactive materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,920.00
inventory 250mg
10-20 days ฿20,240.00

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2,5-Dimethoxybenzene-1,4-diol
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Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pharmaceuticals. It serves as a building block in the development of antioxidants due to its phenolic structure, which can scavenge free radicals. Also employed in research settings for the synthesis of substituted quinones, which have applications in materials science and bioactive compound development. Its electron-rich aromatic system makes it useful in the study of charge-transfer complexes and electroactive mat

Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pharmaceuticals. It serves as a building block in the development of antioxidants due to its phenolic structure, which can scavenge free radicals. Also employed in research settings for the synthesis of substituted quinones, which have applications in materials science and bioactive compound development. Its electron-rich aromatic system makes it useful in the study of charge-transfer complexes and electroactive materials.

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