Molecular structure of trans-1,2-Cyclohexanedicarboxylic acid, CAS Number: 2305-32-0
trans-1,2-Cyclohexanedicarboxylic acid (CAS 2305-32-0)
CAS Number:
2305-32-0
Molecular Weight:
172.18
Molecular Formula:
C8H12O4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Trans-1,2-Cyclohexanedicarboxylic acid (trans-1,2-CHDA) holds significant importance in the chemical industry. This cyclic dicarboxylic acid features a trans-configuration of its two carboxylic acid groups. In scientific research and development, Trans-1,2-Cyclohexanedicarboxylic acid finds extensive usage. It serves as a key component in synthesizing various compounds. Furthermore, it acts as a catalyst for ester and amide hydrolysis and serves as a building block for polymer synthesis. The versatility and importance of Trans-1,2-Cyclohexanedicarboxylic acid arise from its distinctive properties and reactivity. Its ability to form hydrogen bonds with other molecules facilitates diverse reactions.
trans-1,2-Cyclohexanedicarboxylic acid (CAS 2305-32-0) References
- The 1:1 adduct of hexamethylenetetramine (HMT) with racemic trans-1,2-cyclohexanedicarboxylic acid (CDA). | Venkatraman, R., et al. 2004. Acta Crystallogr C. 60: o633-5. PMID: 15345840
- Acylation of phenol by cyclic and acyclic anhydrides in anhydrous acetic acid. | Haddadin, MJ., et al. 1975. J Pharm Sci. 64: 1766-70. PMID: 172623
- The N domain of human angiotensin-I-converting enzyme: the role of N-glycosylation and the crystal structure in complex with an N domain-specific phosphinic inhibitor, RXP407. | Anthony, CS., et al. 2010. J Biol Chem. 285: 35685-93. PMID: 20826823
- One-dimensional hydrogen-bonded infinite chain from nickel(II) tetraaza macrocyclic complex and 1,2-cyclopentanedicarboxylate ligand. | Lim, IT. and Choi, KY. 2011. Int J Mol Sci. 12: 2232-41. PMID: 21731438
- Simple and efficient methods for discrimination of chiral diacids and chiral alpha-methyl amines. | Chaudhari, SR. and Suryaprakash, N. 2012. Org Biomol Chem. 10: 6410-9. PMID: 22735343
- The role of the alcohol and carboxylic acid in directed ruthenium-catalyzed C(sp3)-H α-alkylation of cyclic amines. | Bergman, SD., et al. 2012. Chemistry. 18: 10393-8. PMID: 22786664
- Genome and Phenotype Microarray Analyses of Rhodococcus sp. BCP1 and Rhodococcus opacus R7: Genetic Determinants and Metabolic Abilities with Environmental Relevance. | Orro, A., et al. 2015. PLoS One. 10: e0139467. PMID: 26426997
- Silica sol assisted chromatographic NMR spectroscopy for resolution of trans- and cis-isomers. | Yang, Y., et al. 2016. J Magn Reson. 265: 210-4. PMID: 26942864
- Super-complexes of adhesion GPCRs and neural guidance receptors. | Jackson, VA., et al. 2016. Nat Commun. 7: 11184. PMID: 27091502
- Coordination Polymers and Cage-Containing Frameworks in Uranyl Ion Complexes with rac- and (1R,2R)-trans-1,2-Cyclohexanedicarboxylates: Consequences of Chirality. | Thuéry, P. and Harrowfield, J. 2017. Inorg Chem. 56: 1455-1469. PMID: 28060503
- Recognition of Hydrophilic Cyclic Compounds by a Water-Soluble Cavitand. | Wan, YH., et al. 2021. Molecules. 26: PMID: 33808102
- Metabolic Profiling Identifies Changes in the Winter Wheat Grains Following Fusarium Treatment at Two Locations in Croatia. | Sunic, K., et al. 2023. Plants (Basel). 12: PMID: 36840259
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
trans-1,2-Cyclohexanedicarboxylic acid, 5 g | sc-280145 | 5 g | $106.00 |