6843-76-1

Usage

Uses

Used in Scientific Research:
1,1,6,6-D4-1,6-HEXANDIOL is used as a research compound for [application reason] in the field of [application industry]. Its isotopically labeled nature allows for enhanced tracking and analysis of chemical reactions and processes, making it a valuable tool for studying complex biological systems and mechanisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1,1,6,6-D4-1,6-HEXANDIOL is used as a research compound for drug discovery and development. Its unique properties enable researchers to investigate the interactions between drug molecules and biological targets, leading to the identification of potential therapeutic agents and the optimization of drug candidates.
Used in Analytical Chemistry:
1,1,6,6-D4-1,6-HEXANDIOL is utilized as a reference material or internal standard in analytical chemistry. Its stable isotopic composition ensures accurate measurements and quantification of target compounds in complex samples, improving the reliability and precision of analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.

Upstream product

• 629-11-8 1,6-hexanediol 
• 627-93-0 hexanedioic acid dimethyl ester 

Relevant academic research and scientific papers

SUBSTITUTED ETHANOLAMINES

The present invention relates to new substituted ethanolamine adrenergic receptor modulators, pharmaceutical compositions thereof, and methods of use thereof.

A convenient and effective method for the regioselective deuteration of alcohols

The convenient and regioselective deuteration of hydroxy groups on vicinal carbons was achieved by the combination of 5% ruthenium on carbon (Ru/C), hydrogen gas and deuterium oxide (D2O).

Solid-state NMR investigations on urea inclusion compounds: Order and dynamics of 1,6-dibromohexane

The molecular properties of 1,6-dibromohexane in its urea inclusion compound are investigated by means of a multinuclear solid-state NMR spectroscopy. 13C CP/MAS and 1H MAS NMR studies (line shapes, spin-lattice relaxation measurements) were performed for the first time to probe the guest dynamics and conformational order. Variable temperature 2H NMR studies comprising line shape analysis as well as spin-lattice relaxation (T1Z, T1Q) experiments were done on samples with guest molecules selectively deuterated at two different positions. A quantitative analysis of the experimental data proves that the guest dynamics are dominated by mutual exchange between two gauche conformers. It is shown that these guest motions unequivocally can be quantified (type and time-scale) by a comprehensive analysis of the T1Z and T1Q data. In addition, there is evidence that other motional contributions, such as overall molecular fluctuations and lateral motions, also contribute to spin relaxation. The molecular behaviour of 1,6-dibromohexane in urea is completely different from that reported for the long chain analogues or for n-alkanes where typically unhindered overall rotational motions of the guests in their all-trans conformation around the urea channel long axis are discussed. The differences in guest ordering and dynamics are a direct consequence of the differences of the urea lattice structures (monoclinic vs. hexagonal urea lattice).

The mechanisms of n-butyllithium induced β-cleavage of 2-methyltetrahydrofuran and oxepane

The n-butyllithium induced β-cleavage reactions of 2-methyltetrahydrofuran and oxepane operate via different mechanisms. 2-Methyltetrahydrofuran undergoes an E2 elimination, whilst oxepane undergoes an α,β′-elimination involving initial deprotonation at the α-position followed by a transannular hydrogen transfer.