100790-31-6 Usage
Description
<2,6-13C2>phenol is a chemical compound that is a labeled version of phenol, a commonly used compound in the production of various chemicals and materials. The <2,6-13C2> prefix indicates that the carbon atoms at positions 2 and 6 in the phenol molecule have been replaced with the carbon-13 isotope, which has two extra neutrons compared to the more common carbon-12. This labeling is often used in research and industrial applications to track the movement and transformation of the phenol molecule in different chemical processes. Additionally, the presence of labeled carbon atoms can also provide important information about the specific reactions and pathways by which phenol is processed and metabolized in biological systems. Overall, <2,6-13C2>phenol is a valuable tool for studying the behavior and applications of phenol in various scientific and industrial contexts.
Uses
Used in Research and Development:
<2,6-13C2>phenol is used as a research tool for tracking the movement and transformation of phenol molecules in various chemical processes. The presence of the carbon-13 isotope allows scientists to monitor the behavior of phenol in different reactions and pathways, providing valuable insights into its applications and potential uses.
Used in Industrial Applications:
<2,6-13C2>phenol is used as a labeled compound in industrial processes to study the specific reactions and pathways by which phenol is processed and metabolized. This information can be used to optimize the production of various chemicals and materials derived from phenol, leading to more efficient and cost-effective manufacturing processes.
Used in Pharmaceutical Industry:
<2,6-13C2>phenol can be used as a labeled compound in the development of new drugs and therapies that involve phenol or its derivatives. The ability to track the movement and transformation of phenol in biological systems can help researchers understand the mechanisms of action of these drugs and design more effective treatments.
Used in Environmental Studies:
<2,6-13C2>phenol can be used as a labeled compound in environmental studies to investigate the fate and transport of phenol in the environment. This information can be used to assess the potential risks and impacts of phenol and its derivatives on ecosystems and human health, and to develop strategies for mitigating these risks.
Check Digit Verification of cas no
The CAS Registry Mumber 100790-31-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,7,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100790-31:
(8*1)+(7*0)+(6*0)+(5*7)+(4*9)+(3*0)+(2*3)+(1*1)=86
86 % 10 = 6
So 100790-31-6 is a valid CAS Registry Number.
100790-31-6Relevant articles and documents
An Efficient Chemomicrobiological Synthesis of Stable Isotope-Labeled L-Tyrosine and L-Phenylalanine
Walker, T. E.,Matheny, C.,Storm, C. B.,Hayden, H.
, p. 1175 - 1179 (2007/10/02)
L-Tyrosine specifically labeled with 2H, 13C, 18O, or 15N has been synthesized by using a combination of organic synthetic methods and the β-tyrosinase enzyme activity of the bacterium Erwinia herbicola.The following L-tyrosine isotopomers were prepared: L-tyrosine from phenol and L-serine, L-tyrosine from phenol and L-serine, L-tyrosine from phenol and L-serine, L-tyrosine from ammonium sulfate, phenol, and pyruvate, and L-tyrosine from phenol and L-serine.The β-tyrosinase activitywas also used to prepare 2'-fluoro-L-tyrosine and 3'-fluoro-L-tyrosine from 3-fluorophenol and 2-fluorophenol, respectively.Phenol enriched with 13C was prepared by the condensation of acetone with nitromalonaldehyde, reduction of the resulting p-nitrophenol to p-aminophenol, and reductive removal of the nitrogen from the diazonium salt to form either - or phenol in a 40percent overall yield from acetone.The yields of L-tyrosine were typically around 90percent from labeled phenol.Labeled L-phenylalanine was chemically prepared from L-tyrosine in a 75percent overall yield.This was deemed the best approach to labeled L-phenylalanine, given the efficient method for preparing L-tyrosine from phenol.The approach to labeled L-phenylalanine represents a unique combination of chemical synthesis (phenol), biosynthesis (L-tyrosine), and finally chemical synthesis (L-phenylalanine).The chirality is introduced by the biochemical step, obviating the need for elaborate and inherently inefficient chiral manipulations.
