2,7-Dimethoxy-1,4-naphthoquinone

95%

Reagent Code: #167885
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CAS Number 6223-34-3

science Other reagents with same CAS 6223-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.4058 g/mol
Formula C₂₂H₁₉N₃O
thermostat Physical Properties
Melting Point 214-215 °C
Boiling Point 409.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.29±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pigments. It serves as a building block in the development of functional materials for electrochemical applications due to its redox-active quinone structure. Also investigated for use in photovoltaic systems and as a model compound in studies of electron transfer processes. Its derivatives show potential in pharmaceutical research, especially in the design of compounds with antimicrobial and antitumor activities.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿57,600.00
inventory 250mg
10-20 days ฿96,000.00

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2,7-Dimethoxy-1,4-naphthoquinone
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Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pigments. It serves as a building block in the development of functional materials for electrochemical applications due to its redox-active quinone structure. Also investigated for use in photovoltaic systems and as a model compound in studies of electron transfer processes. Its derivatives show potential in pharmaceutical research, especially in the design of compounds with antimicrobial and antitumor activities.

Used as an intermediate in organic synthesis, particularly in the preparation of dyes and pigments. It serves as a building block in the development of functional materials for electrochemical applications due to its redox-active quinone structure. Also investigated for use in photovoltaic systems and as a model compound in studies of electron transfer processes. Its derivatives show potential in pharmaceutical research, especially in the design of compounds with antimicrobial and antitumor activities.

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