3S-(3a,3a,6a)-Hexahydrofuro[2,3-b]furan-3-ol acetate, identified by its CAS number 162020-29-3, is a chemical compound characterized by its unique bicyclic structure, which includes a furan ring fused to a cyclopentane moiety. This compound features a hydroxyl group (-OH) and an acetate group (-OCOCH3), contributing to its reactivity and potential applications in organic synthesis. The stereochemistry indicated by the "3S" designation suggests specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. Typically, such compounds may exhibit properties relevant to medicinal chemistry, including potential use as intermediates in the synthesis of pharmaceuticals or as bioactive agents. The presence of the furan ring often suggests potential for aromaticity and reactivity in electrophilic substitution reactions. Overall, the characteristics of this compound make it a subject of interest in various fields, including organic chemistry and pharmacology, although specific applications would depend on further research and exploration of its properties.

3S-(3a,3a,6a)]-Hexahydrofuro[2,3-b]furan-3-ol Acetate

162020-29-3: (3S,3aR,6aS)-Hexahydro-furo[2,3-b]furan-3-ol Acetate, (3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-yl Acetate

Furo[2,3-b]furan-3-ol, hexahydro-, 3-acetate, (3S,3aR,6aS)-

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(3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-yl acetate

Applications Darunavir intermediate.
References Ghosh, A., et al.: J. Med. Chem., 39, 3278 (1996), Ghosh, A., et al.: Bioorg. Med. Chem. Lett., 1998, 8, 687 (1998), Richman, D., et al.: Nature, 410, 995 (2001), Koh, Y., et al.: Antimicrob. Agents Chemother., 47, 3123 (2003),


CAS 162020-29-3: 3S-(3a,3a,6a)]-Hexahydrofuro[2,3-b]furan-3-ol Acetate

Furo[2,3-b]furan-3-ol, hexahydro-, 3-acetate, (3S,3aR,6aS)-

Ref: IN-DA001SNJ

(3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-yl acetate

Ref: 3D-FH23801

(3S,3aR,6aS)-Hexahydrofuro[2,3-b]furan-3-yl Acetate

Ref: TR-H293980