1,3-Bis(2-acetyl-3-hydroxyphenoxy)-2-hydroxypropane

• CAT Number: R023505
• CAS Number: 16150-44-0
• Molecular Formula: C19H20O7
• Molecular Weight: 360.36
• Purity: ≥95%
• Synonyms: USP Cromolyn Sodium Related Compound A; 1,3-Bis(2-acetyl-3-hydroxyphenoxy)-2-propanol; 2’,2’’’-[(2-Hydroxytrimethylene)dioxy]bis[6’-hydroxyacetophenone
• Storage: -20°C
• IUPAC Name: 1-[2-[3-(2-acetyl-3-hydroxyphenoxy)-2-hydroxypropoxy]-6-hydroxyphenyl]ethanone
• InChI: InChI=1S/C19H20O7/c1-11(20)18-14(23)5-3-7-16(18)25-9-13(22)10-26-17-8-4-6-15(24)19(17)12(2)21/h3-8,13,22-24H,9-10H2,1-2H3
• InChIKey: RUOPAUDVYRHXDB-UHFFFAOYSA-N
• SMILES: CC(=O)C1=C(C=CC=C1OCC(COC2=CC=CC(=C2C(=O)C)O)O)O

1,3-Bis(2-acetyl-3-hydroxyphenoxy)-2-hydroxypropane(CAT: R023505) is a multifunctional aromatic ether featuring a glycerol-based backbone substituted with two acetylated hydroxyphenyl groups. This compound combines phenolic and ketone functionalities, offering sites for further chemical modification or polymerization. Its structural characteristics make it useful as an intermediate in the synthesis of advanced polymers, resins, or bioactive molecules. The presence of both hydroxyl and acetyl groups allows for tailored reactivity in cross-linking, esterification, or coordination chemistry. It may also serve in the development of antioxidant materials or as a building block in pharmaceutical and cosmetic formulations requiring multifunctional, aromatic-rich components with potential bioactivity or stability.