68661-15-4 Usage
Uses
Used in Research and Analytical Studies:
PHENYL(ACETIC ACID-2-13C) is used as a tracer or labeled compound for tracking metabolic pathways and chemical reactions. It aids researchers in understanding the mechanisms of various processes and provides insights into molecular interactions and transformations within biological systems.
Used in Pharmacology:
In the field of pharmacology, PHENYL(ACETIC ACID-2-13C) is utilized as a labeled compound to study drug metabolism, distribution, and excretion. It helps researchers identify and analyze the metabolic products of drugs, contributing to the development of safer and more effective medications.
Used in Biochemistry:
PHENYL(ACETIC ACID-2-13C) is employed in biochemistry as a labeled compound for investigating enzyme mechanisms, substrate specificity, and metabolic pathways. It enables researchers to gain a deeper understanding of enzyme-catalyzed reactions and their role in biological processes.
Used in Organic Chemistry:
In organic chemistry, PHENYL(ACETIC ACID-2-13C) is used as a labeled compound for studying reaction mechanisms, reaction kinetics, and the synthesis of complex organic molecules. It assists researchers in elucidating the details of chemical reactions and optimizing reaction conditions for the production of desired compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 68661-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,6 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68661-15:
(7*6)+(6*8)+(5*6)+(4*6)+(3*1)+(2*1)+(1*5)=154
154 % 10 = 4
So 68661-15-4 is a valid CAS Registry Number.
68661-15-4Relevant academic research and scientific papers
Partial oxygen migration in the photochemical wolff rearrangement - α-Oxocarben-Oxiren-isomerization or intermolecular mechanism?
Haiss, Peter,Zeller, Klaus-Peter
, p. 595 - 605 (2007/10/03)
Crossover experiments between isotopomeric species of 2-diazo-1-oxo-1-phenylethane (18O, 13C, D) establish beyond doubt that the oxygen migration accompanying the photochemical Wolff rearrangement is not the result of intermolecular
Dissociative ionization of aryl-substituted vinyl bromides in the gas phase: Experimental and computational evidence for the formation of stable α-arylvinyl cations both by direct means and spontaneous exothermic isomerization of unstable isomeric ions
Apeloig, Yitzhak,Franke, Wilfried,Rappoport, Zvi,Schwarz, Helmut,Stahl, Daniel
, p. 2770 - 2780 (2007/10/02)
The kinetic energy release T which accompanies the Br· loss from ionized (E)- and (Z)-β-bromostyrenes (5 and 6) in the gas phase is higher by 0.7 ± 0.03 kcal mol-1 than that from the molecular ion of α-bromostyrene (4). Together with both colli
