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Home  > rel-(E)-3-((2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde

AE17471

118916-57-7 | rel-(E)-3-((2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde

Packsize Purity Availability Price Discounted Price    Quantity
1mg 95% 2 weeks $336.00 $235.00 -   +
5mg 95% 2 weeks $1,251.00 $876.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE17471
Chemical Name: rel-(E)-3-((2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde
CAS Number: 118916-57-7
Molecular Formula: C20H20O6
Molecular Weight: 356.3692
MDL Number: MFCD20260538
SMILES: O=C/C=C/c1cc2c(c(c1)OC)O[C@@H]([C@H]2CO)c1ccc(c(c1)OC)O

 

Upstream Synthesis Route
  • The rel-(E)-3-((2S,3R)-2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)acrylaldehyde is a versatile compound commonly used in chemical synthesis processes. Its functionality as an acrylaldehyde derivative makes it a valuable building block for the synthesis of various organic molecules. This compound can participate in a range of reactions such as aldol condensation, Michael addition, and Wittig reaction, allowing for the formation of complex structures with specific stereochemical configurations. Its unique structural features, including the presence of a dihydrobenzofuran ring and a hydroxymethyl group, offer strategic opportunities in the design and assembly of bioactive compounds, natural product analogs, and pharmaceutical intermediates. The controlled manipulation of its reactive sites enables chemists to access diverse molecular scaffolds with enhanced properties and functionalities, making it a key component in the toolbox of synthetic chemists.
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