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Updated: May 31, 2026
09:45
Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
Published on: April 27, 2017
1-Cyclo-hexyl-sulfinyl-2-methyl-naphtho-[2,1-b]furan
Summary
This study details the molecular structure of a novel organic compound, C(19)H(20)O(2)S. The research highlights the compound
Area of Science:
- Crystallography
- Organic Chemistry
- Supramolecular Chemistry
Background:
- Understanding molecular conformation and intermolecular interactions is crucial in predicting material properties.
- Sulfinyl groups are important functional groups in various organic molecules.
Purpose of the Study:
- To elucidate the crystal structure and molecular conformation of the title compound, C(19)H(20)O(2)S.
- To investigate the intermolecular interactions present in the crystalline state.
Main Methods:
- Single-crystal X-ray diffraction was employed to determine the three-dimensional structure.
- Analysis of bond lengths, bond angles, and intermolecular contacts.
Main Results:
- The cyclo-hexyl ring adopts a chair conformation.
- The aryl-sulfinyl moiety is equatorially oriented.
- Weak intermolecular C-H⋯O hydrogen bonds link the molecules in the crystal.
- The sulfinyl oxygen atom exhibits disorder over two orientations.
Conclusions:
- The study provides detailed structural information about the title compound.
- The observed conformation and intermolecular interactions offer insights into crystal packing and potential reactivity.
- The sulfinyl group disorder suggests conformational flexibility in the solid state.
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