1-Acetyl-2,6-dihydroxynaphthalene

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Reagent Code: #171786
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CAS Number 108804-50-8

science Other reagents with same CAS 108804-50-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.21 g/mol
Formula C₁₂H₁₀O₃
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MDL Number MFCD24725628
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of naphthoquinone-based dyes and pigments, particularly in the production of high-performance organic semiconductors and photoresists. It plays a role in the development of specialty polymers with enhanced thermal and oxidative stability. Also employed in research for photochromic materials due to its ability to undergo reversible light-induced transformations. Its hydroxyl and acetyl functional groups allow for derivatization in pharmaceutical and agrochemical applications, especially in the design of bioactive molecules with antioxidant properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,740.00
inventory 1g
10-20 days ฿12,248.50

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1-Acetyl-2,6-dihydroxynaphthalene
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Used as an intermediate in the synthesis of naphthoquinone-based dyes and pigments, particularly in the production of high-performance organic semiconductors and photoresists. It plays a role in the development of specialty polymers with enhanced thermal and oxidative stability. Also employed in research for photochromic materials due to its ability to undergo reversible light-induced transformations. Its hydroxyl and acetyl functional groups allow for derivatization in pharmaceutical and agrochemical appli
Used as an intermediate in the synthesis of naphthoquinone-based dyes and pigments, particularly in the production of high-performance organic semiconductors and photoresists. It plays a role in the development of specialty polymers with enhanced thermal and oxidative stability. Also employed in research for photochromic materials due to its ability to undergo reversible light-induced transformations. Its hydroxyl and acetyl functional groups allow for derivatization in pharmaceutical and agrochemical applications, especially in the design of bioactive molecules with antioxidant properties.
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