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CAS 24327-08-0

:

rel-(3aR,4S,7R,7aS)-3a,4,7,7a-Tetrahydro-4,7-ethanoisobenzofuran-1,3-dione

Description:
The chemical substance known as rel-(3aR,4S,7R,7aS)-3a,4,7,7a-Tetrahydro-4,7-ethanoisobenzofuran-1,3-dione, with the CAS number 24327-08-0, is a bicyclic compound characterized by its unique fused ring structure. This compound features a tetrahydrobenzofuran moiety, which contributes to its potential biological activity. The presence of the dione functional groups indicates that it has two carbonyl groups, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. The stereochemistry, denoted by the rel- and specific R/S configurations, suggests that the compound has multiple chiral centers, which may influence its pharmacological properties and interactions with biological targets. Such compounds are often of interest in medicinal chemistry due to their potential therapeutic applications. Additionally, the compound's solubility, stability, and reactivity can be influenced by its structural features, making it a candidate for further research in organic synthesis and drug development.
Formula:C10H10O3
InChI:InChI=1/C10H10O3/c11-9-7-5-1-2-6(4-3-5)8(7)10(12)13-9/h1-2,5-8H,3-4H2/t5-,6+,7-,8+
InChI key:InChIKey=YIHKILSPWGDWPR-KVFPUHGPNA-N
SMILES:O=C1[C@@]2([C@@]([C@@]3(C=C[C@]2(CC3)[H])[H])(C(=O)O1)[H])[H]
Synonyms:
  • 4,7-Ethanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aR,4S,7R,7aS)-rel-
  • Bicyclo[2.2.2]octene-2,3-endo-dicarboxylic anhydride
  • Bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride, cis-endo-
  • 4,7-Ethanoisobenzofuran-1,3-dione, 3a,4,7,7a-tetrahydro-, (3aα,4α,7α,7aα)-
  • rel-(3aR,4S,7R,7aS)-3a,4,7,7a-Tetrahydro-4,7-ethanoisobenzofuran-1,3-dione
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