2,3-Dichloro-1,4-naphthoquinone

Analyze the control, ≥99%

Reagent Code: #169518
label
Alias 2,3-dichloro-1,4-naphthoquinone;dichloronaphthoquinone
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CAS Number 117-80-6

science Other reagents with same CAS 117-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.04 g/mol
Formula C₁₀H₄Cl₂O₂
badge Registry Numbers
EC Number 204-210-5
MDL Number MFCD00001677
thermostat Physical Properties
Melting Point 194-197 °C(lit.)
Boiling Point 275 °C (2 mmHg)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing naphthoquinone-based colorants. It serves as a building block in organic synthesis for pharmaceuticals and agrochemicals due to its reactive quinone structure. Also employed in the development of electroactive materials and as a catalyst or reagent in oxidation reactions. Its electron-deficient ring system makes it useful in the preparation of functional polymers and charge-transfer complexes.

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inventory 250mg
10-20 days ฿2,550.00

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2,3-Dichloro-1,4-naphthoquinone
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Used as an intermediate in the synthesis of dyes and pigments, particularly for producing naphthoquinone-based colorants. It serves as a building block in organic synthesis for pharmaceuticals and agrochemicals due to its reactive quinone structure. Also employed in the development of electroactive materials and as a catalyst or reagent in oxidation reactions. Its electron-deficient ring system makes it useful in the preparation of functional polymers and charge-transfer complexes.
Used as an intermediate in the synthesis of dyes and pigments, particularly for producing naphthoquinone-based colorants. It serves as a building block in organic synthesis for pharmaceuticals and agrochemicals due to its reactive quinone structure. Also employed in the development of electroactive materials and as a catalyst or reagent in oxidation reactions. Its electron-deficient ring system makes it useful in the preparation of functional polymers and charge-transfer complexes.
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