334689-56-4 Usage
Uses
Used in Chemical Synthesis:
Cyclohexanone-13C6 is used as a labeled intermediate for the synthesis of various organic compounds. The incorporation of 13C atoms allows for the tracking of the compound's fate in complex reaction mixtures and can provide valuable insights into reaction mechanisms and pathways.
Used in Analytical Chemistry:
In analytical chemistry, Cyclohexanone-13C6 serves as a labeled reference material for the calibration of mass spectrometry and nuclear magnetic resonance (NMR) instruments. The presence of 13C atoms can enhance the detection sensitivity and accuracy of these analytical techniques, particularly when studying isotopically labeled compounds or mixtures.
Used in Research and Development:
Cyclohexanone-13C6 is used as a research tool for investigating the metabolic pathways and biotransformation processes involving cyclohexanone in biological systems. The isotopic labeling can help researchers differentiate between the labeled compound and its natural counterparts, providing a clearer understanding of the underlying biochemical processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Cyclohexanone-13C6 can be employed as a labeled starting material or intermediate for the synthesis of isotopically labeled drug candidates. This can be particularly useful for studying the pharmacokinetics, pharmacodynamics, and metabolic profiles of new drug molecules in preclinical and clinical research.
Used in Environmental Science:
Cyclohexanone-13C6 can be utilized in environmental science applications to study the fate and transport of cyclohexanone and its derivatives in the environment. The isotopic labeling can help researchers track the compound's behavior in various environmental matrices, such as soil, water, and air, and assess its potential impact on ecosystems and human health.
Used in Material Science:
In material science, Cyclohexanone-13C6 can be used to study the interactions between cyclohexanone and other materials, such as polymers and catalysts. The isotopic labeling can provide valuable information on the adsorption, diffusion, and reaction processes occurring at the molecular level, which can be crucial for the design and optimization of new materials and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 334689-56-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,4,6,8 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 334689-56:
(8*3)+(7*3)+(6*4)+(5*6)+(4*8)+(3*9)+(2*5)+(1*6)=174
174 % 10 = 4
So 334689-56-4 is a valid CAS Registry Number.
334689-56-4Relevant academic research and scientific papers
Ellames, George J.,Herbert, John M.
, p. 169 - 172 (2001)
An efficient route is described for the preparation of [13C6]-ε-caprolactam 81b), and thence to [13C6]-hexamethyleneimine (2b) hydrochloride. The sequence, from [13C6]-phenol, uses a rhodium-catalysed hydrogenation to generate labelled cyclohexanol, and thence cyclohexanone, whose oxime was subjected to a Beckmann rearrangement to give 1a.
