Properties and Exciting Facts About 610-09-3

Although many compounds look similar to this compound(610-09-3)Synthetic Route of C8H12O4, numerous studies have shown that this compound(SMILES:O=C([C@H]1[C@@H](C(O)=O)CCCC1)O), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

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.Synthetic Route of C8H12O4.Chandramalar, A. V. M.; Lim, Y. Y.; Leong, Y. K. published the article 《The effects of cis-trans configuration of cyclohexane multi-carboxylic acids on colloidal forces in dispersions: steric, hydrophobic and bridging》 about this compound( cas:610-09-3 ) in Colloids and Surfaces, A: Physicochemical and Engineering Aspects. Keywords: configuration effect cyclohexanecarboxylic acid zirconia colloidal force; yield stress pH zirconia cyclohexanecarboxylic acid configuration effect. Let’s learn more about this compound (cas:610-09-3).

The effects of cis- and trans-1,2-, trans-1,4-cyclohexanedicarboxylic acid, 95% cis-1,3,5-cyclohexane tricarboxylic acid and cis-1,2,3,4,5,6-cyclohexanehexacarboxylic acid on the yield stress-pH behavior of concentrated ZrO2 dispersions are reported. Adsorbed cis-1,2,3,4,5,6-cyclohexanehexacarboxylic acid imparts predominantly steric interactions. It forms a steric barrier keeping the interacting particles apart. Adsorbed cis- and trans-1,2 increase the maximum yield stress and this was attributed to a hydrophobic force resulting from the part of the cyclohexane ring sticking out into the solution which is devoid of charged or hydrophilic group. Adsorbed trans-1,4 increases the maximum yield stress by ≥3-fold and its configuration favors strong bridging interaction with an adjacent particle. Predominantly, cis-1,3,5 also increases the maximum yield stress but only by 60% at the same additive concentration This was attributed to a smaller degree of bridging.

Although many compounds look similar to this compound(610-09-3)Synthetic Route of C8H12O4, numerous studies have shown that this compound(SMILES:O=C([C@H]1[C@@H](C(O)=O)CCCC1)O), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Benzisoxazole – Wikipedia,
Benzisoxazole – an overview | ScienceDirect Topics