1-(4-(Benzyloxy)-2-hydroxy-6-methoxyphenyl)ethanone

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Reagent Code: #149796
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CAS Number 39548-89-5

science Other reagents with same CAS 39548-89-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.29 g/mol
Formula C₁₆H₁₆O₄
badge Registry Numbers
MDL Number MFCD09955327
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules, particularly in the development of flavonoids and other polyphenolic compounds with potential antioxidant and anti-inflammatory properties. Its protected hydroxyl and methoxy groups allow selective reactions in multi-step syntheses. Also employed in research settings for designing enzyme inhibitors and studying structure-activity relationships in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,110.00
inventory 250mg
10-20 days ฿6,170.00
inventory 1g
10-20 days ฿15,320.00

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1-(4-(Benzyloxy)-2-hydroxy-6-methoxyphenyl)ethanone
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules, particularly in the development of flavonoids and other polyphenolic compounds with potential antioxidant and anti-inflammatory properties. Its protected hydroxyl and methoxy groups allow selective reactions in multi-step syntheses. Also employed in research settings for designing enzyme inhibitors and studying structure-activity relationships in me

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It serves as a building block in the preparation of bioactive molecules, particularly in the development of flavonoids and other polyphenolic compounds with potential antioxidant and anti-inflammatory properties. Its protected hydroxyl and methoxy groups allow selective reactions in multi-step syntheses. Also employed in research settings for designing enzyme inhibitors and studying structure-activity relationships in medicinal chemistry.

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