What about chemistry interests you the most 87-41-2

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An article Squaramide-Catalyzed Asymmetric Intramolecular Oxa-Michael Reaction of alpha,beta-Unsaturated Carbonyls Containing Benzyl Alcohol: Construction of Chiral 1-Substituted Phthalans WOS:000649101400068 published article about ENANTIOSELECTIVE SYNTHESIS; ORGANOCATALYSTS; BOND; 1,3-DIHYDROISOBENZOFURANS; STRATEGY; CASCADE in [Son, Eun Chae; Kim, Seung Yeon; Kim, Sung-Gon] Kyonggi Univ, Coll Nat Sci, Dept Chem, Suwon 16227, South Korea in 2021, Cited 50. The Name is Isobenzofuran-1(3H)-one. Through research, I have a further understanding and discovery of 87-41-2. Formula: C8H6O2

Organocatalytic enantioselective intramolecular oxa-Michael reactions of benzyl alcohol bearing alpha,beta-unsaturated carbonyls as Michael acceptors are presented herein. Using cinchona squaramide-based organocatalyst, enones as well as alpha,beta-unsaturated esters containing benzyl alcohol provided their corresponding 1,3-dihydroisobenzofuranyl-1-methylene ketones and 1,3-dihydroisobenzofuranyl-1-methylene esters in excellent yields with high enantioselectivities. In addition, enantioenriched 1,3-dihydroisobenzofuranyl-1-methylene ketone could be obtained from the Wittig/oxa-Michael reaction cascade of 1,3-dihydro-2-benzofuran-1-ol.

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Reference:
Benzofuran – Wikipedia,
,Benzofuran | C8H6O – PubChem