2-Hydroxy-1-(4-methoxyphenyl)-2-phenylethanone

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Reagent Code: #132817
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CAS Number 4254-17-5

science Other reagents with same CAS 4254-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 242.27 g/mol
Formula C₁₅H₁₄O₃
badge Registry Numbers
MDL Number MFCD00016852
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of chiral compounds for drug development. It serves as a building block in asymmetric synthesis due to the presence of both hydroxyl and carbonyl functional groups, which allow for selective transformations. Commonly employed in the production of analgesics and anti-inflammatory agents. Also utilized in the development of photoinitiators for polymer chemistry, where it contributes to light-induced curing processes in coatings, inks, and adhesives. Its aromatic structure enhances UV absorption, making it suitable for applications requiring photo-reactivity.

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inventory 5g
10-20 days ฿17,970.00

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2-Hydroxy-1-(4-methoxyphenyl)-2-phenylethanone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of chiral compounds for drug development. It serves as a building block in asymmetric synthesis due to the presence of both hydroxyl and carbonyl functional groups, which allow for selective transformations. Commonly employed in the production of analgesics and anti-inflammatory agents. Also utilized in the development of photoinitiators for polymer chemistry, where it contributes to light-induced curing proce

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of chiral compounds for drug development. It serves as a building block in asymmetric synthesis due to the presence of both hydroxyl and carbonyl functional groups, which allow for selective transformations. Commonly employed in the production of analgesics and anti-inflammatory agents. Also utilized in the development of photoinitiators for polymer chemistry, where it contributes to light-induced curing processes in coatings, inks, and adhesives. Its aromatic structure enhances UV absorption, making it suitable for applications requiring photo-reactivity.

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