23034-25-5

Usage

Uses

Used in Chemical Synthesis:
1,4-Cyclohexanedione is used as a key intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and chemical industries. Its high isotopic purity allows for the production of compounds with minimal impurities, ensuring the quality and efficacy of the final products.
Used in Analytical Chemistry:
1,4-Cyclohexanedione, with its high isotopic purity, is utilized in analytical chemistry for the identification and quantification of specific elements or compounds. It can be used as a reference material or in the development of new analytical methods, contributing to the accuracy and reliability of chemical analyses.
Used in Research and Development:
The high isotopic purity of 1,4-cyclohexanedione makes it an essential tool in research and development, particularly in the fields of organic chemistry, materials science, and pharmaceuticals. It can be used to study the properties and behavior of various compounds, leading to the discovery of new materials and drugs.
Used in Isotope Labeling:
1,4-Cyclohexanedione can be used in isotope labeling techniques, where it can be incorporated into compounds to track their movement, distribution, or metabolism in biological systems. This application is particularly useful in the study of metabolic pathways, drug interactions, and the development of targeted therapies.

Upstream product

• 637-88-7 1,4-Cyclohexanedione 

Downstream Products

• 77787-72-5 <2H10>-1,4-cyclohexanediol 
• 73223-81-1 1,4-cyclohexanediol-d12 
• 17647-18-6 1,2,3,4,5,5,6,6-octadeuteriocyclohexa-1,3-diene 
• 40493-71-8 [1,1,2,2,4,4,5,5-D₈]cyclohexane 
• 909409-64-9 [2,2,3,3,5,5,6,6-D₈]1,4-cyclohexanediol di(para-toluenesulfonate) 
• 909409-63-8 [2,2,3,3,5,5,6,6-D₈]1,4-cyclohexanediol 

Relevant academic research and scientific papers

A rhenium-cyclohexane complex with preferential binding of axial C-H bonds: A probe into the relative ability of C-H, C-D, and C-C bonds as hyperconjugative electron donors?

Which bonds bind better? According to NMR experiments with the alkane complex [CpRe(CO)2(cyclohexane)] at low temperatures, complexation with an axial proton is preferred over that through an equatorial one by about 1.5 kJ mol-1. Cal

Classical Organic Reactions in Pure Superheated Water

At high temperatures and pressures, pure liquid water becomes a surprisingly effective medium for the reactions of organic compounds.It may function simultaneously as a convenient solvent, catalyst, and reagent for reactions which are typically acid- or base-catalyzed.Rapid and highly selective conversion are observed for the majority of the compounds in this study.

Bicyclic, Boatlike Cope Rearrangements. Probe for Conformational Preference by the Nodal Carbon Atoms

1,4-Bis(dideuteriomethylene)cyclohexane (1d0) and -cycloheptane (2d0) were rearranged thermally to 1,4-dimethylene-2,2,3,3-tetradeuteriocyclohexane (1d4) and -cycloheptane (2d4), respectively.The Arrhenius parameters for these intramolecular boatlike Cope

Detailed Mechanism of Thermal Hydrogen Migration in Cyclohexadieneiron Tricarbonyl

The thermal isomerization of (cyclohexadiene-5-exo-h-d7)iron tricarbonyl (8) was examined to obtain detailed information about the general mechanism of 1,5-hydrogen shifts in simple cyclic polyolefin iron tricarbonyl complexes.The isotopically labeled sys