6′-Ethoxy-2′-hydroxyacetophenone

≥95%

Reagent Code: #184370
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CAS Number 2750-25-6

science Other reagents with same CAS 2750-25-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₁₀H₁₂O₃
badge Registry Numbers
MDL Number MFCD04974092
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both hydroxyl and acetyl functional groups, enabling derivatization for drug discovery. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and cosmetic formulations, thanks to its ability to absorb ultraviolet light. Its ethoxy and hydroxy substituents enhance solubility and stability in various formulations, making it valuable in both medicinal and industrial chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,880.00
inventory 250mg
10-20 days ฿4,880.00
inventory 1g
10-20 days ฿18,980.00

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6′-Ethoxy-2′-hydroxyacetophenone
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Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both hydroxyl and acetyl functional groups, enabling derivatization for drug discovery. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and cosmetic formulations, thanks to its ability to absorb ultraviolet light. Its ethoxy and hydroxy sub

Used as an intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of nonsteroidal anti-inflammatory drugs (NSAIDs). It serves as a building block in organic reactions due to the presence of both hydroxyl and acetyl functional groups, enabling derivatization for drug discovery. Also employed in the preparation of UV-absorbing compounds for use in sunscreens and cosmetic formulations, thanks to its ability to absorb ultraviolet light. Its ethoxy and hydroxy substituents enhance solubility and stability in various formulations, making it valuable in both medicinal and industrial chemistry.

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