2’,4’-Bis(benzyloxy)acetophenone

≥97%

Reagent Code: #172490
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CAS Number 22877-01-6

science Other reagents with same CAS 22877-01-6

blur_circular Chemical Specifications

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Weight 332.39 g/mol
Formula C₂₂H₂₀O₃
badge Registry Numbers
MDL Number MFCD00101153
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of flavonoids and other polyphenolic compounds. It serves as a protected form of hydroxyacetophenone, allowing selective reactions at other sites in the molecule. Commonly employed in pharmaceutical and agrochemical research where controlled deprotection and coupling steps are required. Its benzyl-protected hydroxyl groups can be removed under mild hydrogenation conditions, making it valuable in multi-step synthesis of bioactive molecules.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,290.00
inventory 5g
10-20 days ฿9,170.00
inventory 25g
10-20 days ฿37,780.00

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2’,4’-Bis(benzyloxy)acetophenone
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Used as an intermediate in organic synthesis, particularly in the preparation of flavonoids and other polyphenolic compounds. It serves as a protected form of hydroxyacetophenone, allowing selective reactions at other sites in the molecule. Commonly employed in pharmaceutical and agrochemical research where controlled deprotection and coupling steps are required. Its benzyl-protected hydroxyl groups can be removed under mild hydrogenation conditions, making it valuable in multi-step synthesis of bioactiv

Used as an intermediate in organic synthesis, particularly in the preparation of flavonoids and other polyphenolic compounds. It serves as a protected form of hydroxyacetophenone, allowing selective reactions at other sites in the molecule. Commonly employed in pharmaceutical and agrochemical research where controlled deprotection and coupling steps are required. Its benzyl-protected hydroxyl groups can be removed under mild hydrogenation conditions, making it valuable in multi-step synthesis of bioactive molecules.

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