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4-(4-Bromo­phenyl)-2,5-diethoxy­carbonyl-6-methyl­thieno­[2,3-b]­pyridine

✍ Scribed by Novoa de Armas, Héctor ;Peeters, Oswald M. ;Blaton, Norbert M. ;De Ranter, Camiel J. ;Suárez Navarro, Margarita ;Salfrán Solano, Esperanza ;Verdecia Reyes, Yamila ;Ochoa Rodríguez, Estael


Publisher
International Union of Crystallography
Year
2003
Tongue
English
Weight
223 KB
Volume
59
Category
Article
ISSN
1600-5368

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📜 SIMILAR VOLUMES


6-Methyl-4-phenyl­thieno­[2,3-b]­pyridin
✍ Novoa de Armas, Héctor ;Peeters, Oswald M. ;Blaton, Norbert M. ;De Ranter, Camie 📂 Article 📅 2003 🏛 International Union of Crystallography 🌐 English ⚖ 207 KB

Single-crystal X-ray study T = 293 K Mean '(C±C) = 0.006 A Ê R factor = 0.055 wR factor = 0.167 Data-to-parameter ratio = 12.5 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.

4-Bromo­phenyl 2,3,4,5,6-penta­bromo­phe
✍ Eriksson, Lars ;Hu, Jiwei 📂 Article 📅 2002 🏛 International Union of Crystallography 🌐 English ⚖ 322 KB

The title compound, C 12 H 4 Br 6 O, belongs to a group of ¯ame retardants known as polybrominated diphenyl ethers (PBDE). Intermolecular BrÁ Á ÁBr contacts in the bc plane give a sheetlike character to the structure of the title compound.

2,2′-Di­bromo-3,3′,4,4′,5,5′,6,6′-octa­m
✍ Karunadasa, Hemamala ;Leggett, Christina ;Wong, Shaun 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 190 KB

The title compound, C 29 H 24 Br 2 , has crystallographic twofold rotation symmetry. The Br atom in the 2 position is disordered with the methyl group in the 6 position. The biphenyl bridge bond distance and the torsion angle between the rings are in good agreement with similar previously reported s

2,3,4,5,6-Penta­bromo­phenyl phenyl ethe
✍ Eriksson, Lars ;Hu, Jiwei 📂 Article 📅 2002 🏛 International Union of Crystallography 🌐 English ⚖ 396 KB

The title compound, C 12 H 5 Br 5 O, belongs to a group of ¯ame retardants known as polybrominated diphenyl ethers (PBDE). Salient features of the packing are stabilization due to intermolecular BrÁ Á ÁBr contacts in the ab plane and aromatic intermolecular contacts along the c direction.