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Chirality in trans-1,4-cyclohexane dicarboxylic acid

✍ Scribed by Máximo Barón

Book ID
103210227
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
403 KB
Volume
240
Category
Article
ISSN
0022-2860

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📜 SIMILAR VOLUMES

trans-1,4-Di­bromo­cyclo­hexane-1,4-di­c
trans-1,4-Di­bromo­cyclo­hexane-1,4-di­carboxyl­ic acid
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Molecules of the title compound, C 8 H 10 Br 2 O 4 , located on symmetry centers, are in a rigid chair conformation, with the COOH and Br substituents axial and equatorial, respectively. The carboxylic acid groups form hydrogen bonds, in a cyclic motif, leading to in®nite chains along the b axis.

(Co-)Polyesters Derived from Isosorbide
(Co-)Polyesters Derived from Isosorbide and 1,4-Cyclohexane Dicarboxylic Acid and Succinic Acid
✍ Mazen Garaleh; Takao Yashiro; Hans R. Kricheldorf; Peter Simon; Saber Chatti 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB

## Abstract The homopolyester of isosorbide and __cis__–__trans__ 1,4‐cyclohexane dicarboxylic acid (CHDA) was prepared by three different methods, but only polycondensation of isosorbide and CHDA dichloride yielded a satisfactory molecular weight (corrected $\overline M \_{\rm n} $ = 11 000 Da). F