The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: cis-Cyclohexane-1,2-dicarboxylic acid( cas:610-09-3 ) is researched.Related Products of 610-09-3.Salakhov, M. S.; Israfilov, A. I.; Gulieva, R. S.; Mamedov, S. A. published the article 《Analysis of the stereochemistry of cyclic dicarboxylic acids by potentiometric titration. IX. Acidic ionization of stereoisomeric cyclic 1,2-dicarboxylic acids in aqueous methanol mixtures》 about this compound( cas:610-09-3 ) in Voprosy Stereokhimii. Keywords: acidity cyclic diacid stereoisomer. Let’s learn more about this compound (cas:610-09-3).
The ionization constants of I-V were determined at 25° for potentiometric titration The cis acids were weaker than the trans acids, and the saturated acids were weaker than the unsaturated ones. The distance between ionizing carboxyls in cis-trans pairs, as calculated by the Ingold method, was apparently the same.
Compounds in my other articles are similar to this one(cis-Cyclohexane-1,2-dicarboxylic acid)Related Products of 610-09-3, you can compare them to see their pros and cons in some ways,such as convenient, effective and so on.
Reference:
Benzisoxazole – Wikipedia,
Benzisoxazole – an overview | ScienceDirect Topics