Description

1-(4-(Benzyloxy)-6-hydroxy-2,3-dimethoxyphenyl)ethanone (CAS No. 25892-95-9) is a high-purity synthetic organic compound with the molecular formula C₁₇H₁₈O₅. This compound, also known by its IUPAC name 1-(6-hydroxy-2,3-dimethoxy-4-phenylmethoxyphenyl)ethanone, features a benzyl-protected phenol group and a ketone functionality, making it a valuable intermediate for pharmaceutical and chemical research. With a molecular weight of 302.32 g/mol, it is supplied as a fine powder or crystalline solid, ensuring consistent quality for laboratory use. Ideal for synthetic organic chemists, this compound is rigorously tested for purity (typically ≥95% by HPLC) and is suitable for use in coupling reactions, medicinal chemistry, and the synthesis of complex heterocycles. Store in a cool, dry place, protected from light and moisture.

Properties

• CAS Number: 25892-95-9
• Complexity: 353
• IUPAC Name: 1-(4-benzyloxy-6-hydroxy-2,3-dimethoxy-phenyl)ethanone
• InChI: InChI=1S/C17H18O5/c1-11(18)15-13(19)9-14(16(20-2)17(15)21-3)22-10-12-7-5-4-6-8-12/h4-9,19H,10H2,1-3H3
• InChI Key: DHPZTYWSWZIJME-UHFFFAOYSA-N
• Exact Mass: 302.11542367
• Molecular Formula: C17H18O5
• Molecular Weight: 302.32
• SMILES: CC(=O)C1=C(C(=C(C=C1O)OCC2=CC=CC=C2)OC)OC
• Topological: 65
• Monoisotopic Mass: 302.11542367
• Synonyms: 25892-95-9, 1-(4-(BENZYLOXY)-6-HYDROXY-2,3-DIMETHOXYPHENYL)ETHANONE, 2-Acetyl-5-(benzyloxy)-3,4-dimethoxyphenol, MFCD15144660, 1-(6-hydroxy-2,3-dimethoxy-4-phenylmethoxyphenyl)ethanone, 1-(4-(benzyloxy)-6-hydroxy-2,3-dimethoxyphenyl)ethan-1-one, 1-[4-(Benzyloxy)-6-hydroxy-2,3-dimethoxyphenyl]ethan-1-one, SCHEMBL16246347, DTXSID60678744, DHPZTYWSWZIJME-UHFFFAOYSA-N, AKOS015891193, AC-7935, SY246443, WS-01577, CS-0198485, 4′-benzyloxy-6′-hydroxy-2′,3′-dimethoxyacetophenone

Application

1-(4-(Benzyloxy)-6-hydroxy-2,3-dimethoxyphenyl)ethanone is primarily used as a key intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research targeting phenolic and methoxy-substituted scaffolds. Its benzyl-protected hydroxyl group allows for selective deprotection in multi-step synthetic routes. Researchers also employ this compound in the development of novel antioxidants and anti-inflammatory agents due to its polyphenolic structure. Additionally, it serves as a precursor for the preparation of advanced materials with potential applications in organic electronics.

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