4'-Benzyloxyacetophenone

98%

Reagent Code: #144415
label
Alias p-benzyloxyacetophenone; 4-benzyloxyacetophenone
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CAS Number 54696-05-8

science Other reagents with same CAS 54696-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.28 g/mol
Formula C₁₅H₁₄O₂
badge Registry Numbers
MDL Number MFCD00017247
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the development of estrogen receptor ligands and other bioactive molecules due to its structural similarity to natural phenolic compounds. Its protected hydroxyl group allows for selective reactions in multi-step syntheses. Also employed in the production of fragrances and specialty polymers where controlled aromatic ketone functionality is required.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Off-white to light yellow solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿300.00
25g
10-20 days ฿480.00
500g
10-20 days ฿3,630.00
100g
10-20 days ฿1,090.00
4'-Benzyloxyacetophenone
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the development of estrogen receptor ligands and other bioactive molecules due to its structural similarity to natural phenolic compounds. Its protected hydroxyl group allows for selective reactions in multi-step syntheses. Also employed in the production of fragrances and specialty polymers where controlled aromatic ketone functionality is required.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the development of estrogen receptor ligands and other bioactive molecules due to its structural similarity to natural phenolic compounds. Its protected hydroxyl group allows for selective reactions in multi-step syntheses. Also employed in the production of fragrances and specialty polymers where controlled aromatic ketone functionality is required.

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