2-HYDROXY-5-BENZYLOXYACETOPHENONE

95%

Reagent Code: #195919
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CAS Number 30992-63-3

science Other reagents with same CAS 30992-63-3

blur_circular Chemical Specifications

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Weight 242.27 g/mol
Formula C₁₅H₁₄O₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of flavonoids and other aromatic compounds with antioxidant properties. Also utilized in the production of photoinitiators for UV-curable resins due to its ability to absorb ultraviolet light. Its benzyl-protected hydroxy group can be selectively deprotected, enabling controlled reactions in multi-step synthetic pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,610.00
inventory 5g
10-20 days ฿16,350.00
inventory 250mg
10-20 days ฿1,380.00

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2-HYDROXY-5-BENZYLOXYACETOPHENONE
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of flavonoids and other aromatic compounds with antioxidant properties. Also utilized in the production of photoinitiators for UV-curable resins due to its ability to absorb ultraviolet light. Its benzyl-protected hydroxy group can be selectiv

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its structure allows for further functionalization, making it valuable in the development of bioactive molecules. Commonly employed in the synthesis of flavonoids and other aromatic compounds with antioxidant properties. Also utilized in the production of photoinitiators for UV-curable resins due to its ability to absorb ultraviolet light. Its benzyl-protected hydroxy group can be selectively deprotected, enabling controlled reactions in multi-step synthetic pathways.

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