March 3, 2026Open Access

5-4- (1 R, 3 S, 4 S) -Neomenthyloxyphenyl-1 H -tetrazole

Key Points

Stability is indicated through three hydrogen bonds linking molecules within the extended structure, enhancing connectivity.
Centroid-centroid distances of 3.5288 Å and 3.6138 Å suggest π-π interactions between phenyl and tetrazole moieties.
The analysis confirms an extended structure with A-ribbons and B-ribbons formed by similar conformers.
Significant hydrogen bonding and aromatic interactions may influence the compound's chemical properties.

Abstract

The monoclinic unit cell of the title compound, C17H24N4O, contains four mol-ecules, two A and two B. In the extended structure, the two similar conformers are connected into A-ribbons and B-ribbons. Three hydrogen bonds connect the mol-ecules within the ribbons, while π-π inter-actions between the phenyl and tetra-zole moieties of different mol-ecules centroid-centroid distances of 3.5288 (11) and 3.6138 (11) Å connect the A and B strands; the aromatic rings are nearly coplanar.

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Cite this study

Detert et al. (Thu,) studied this question.

www.synapsesocial.com/papers/69a75a34c6e9836116a1fc8a — DOI: https://doi.org/10.1107/s2414314626000337

Authors

Heiner Detert

Dieter Schollmeyer

Journals

IUCrData

Actions

Institutions

Johannes Gutenberg University Mainz

References and Citations

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Building similarity graph...

Analyzing shared references across papers

5-4- (1 R, 3 S, 4 S) -Neomenthyloxyphenyl-1 H -tetrazole

Key Points

Abstract

Citation Network

Connected Papers

Discussion

Cite this study

Authors

Journals

Actions

Institutions

References and Citations

Citation Network

Connected Papers

Discussion