68639-73-6 Usage
Description
N-Pentylbenzene-2,3,4,5,6-D5, with the CAS number 68639-73-6, is an isotopically labeled research compound. It is a derivative of pentylbenzene, where five hydrogen atoms are replaced by deuterium atoms, an isotope of hydrogen. N-PENTYLBENZENE-2,3,4,5,6-D5 is primarily used in research settings for various applications due to its unique isotopic properties.
Uses
Used in Research Applications:
N-Pentylbenzene-2,3,4,5,6-D5 is used as an isotopically labeled compound for [application reason]. The deuterium labeling in this compound allows for enhanced detection and tracking in various research experiments, such as studying chemical reactions, metabolic pathways, and molecular interactions.
Used in Chemical Reaction Studies:
In the field of chemistry, N-Pentylbenzene-2,3,4,5,6-D5 is used as a labeled compound for investigating reaction mechanisms and kinetics. The presence of deuterium atoms can help researchers differentiate between various reaction pathways and understand the role of individual atoms in the reaction process.
Used in Metabolic Pathway Research:
In the biological sciences, N-Pentylbenzene-2,3,4,5,6-D5 can be employed as a labeled substrate to study metabolic pathways. The deuterium labeling allows for the tracking of the compound's metabolism and can provide insights into the enzymes and processes involved in its breakdown and utilization.
Used in Molecular Interaction Studies:
N-Pentylbenzene-2,3,4,5,6-D5 is also used as a labeled ligand in the study of molecular interactions, such as protein-ligand binding or receptor-ligand interactions. The isotopic labeling can help researchers determine the binding affinity, specificity, and dynamics of these interactions.
Used in Analytical Chemistry:
In the field of analytical chemistry, N-Pentylbenzene-2,3,4,5,6-D5 can be utilized as an internal standard or a reference compound for quantitative analysis. The deuterium labeling provides a distinct signature that can be used to improve the accuracy and precision of analytical measurements.
Used in Pharmaceutical Research:
N-Pentylbenzene-2,3,4,5,6-D5 can be employed in the pharmaceutical industry for drug discovery and development. N-PENTYLBENZENE-2,3,4,5,6-D5 can be used as a labeled analog of a drug molecule to study its pharmacokinetics, pharmacodynamics, and potential drug-drug interactions.
Used in Environmental Studies:
In environmental science, N-Pentylbenzene-2,3,4,5,6-D5 can be used as a labeled tracer to study the fate and transport of pollutants in the environment. The deuterium labeling can help researchers track the compound's movement and distribution in various environmental matrices, such as soil, water, and air.
Check Digit Verification of cas no
The CAS Registry Mumber 68639-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,6,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68639-73:
(7*6)+(6*8)+(5*6)+(4*3)+(3*9)+(2*7)+(1*3)=176
176 % 10 = 6
So 68639-73-6 is a valid CAS Registry Number.
68639-73-6Relevant articles and documents
Palladium-catalyzed decarboxylation and decarbonylation under hydrothermal conditions: Decarboxylative deuteration
Matsubara, Seijiro,Yokota, Yutaka,Oshima, Koichiro
, p. 2071 - 2073 (2007/10/03)
Equation presented. Decarboxylation of free carboxylic acid was performed by Pd/C catalyst under hydrothermal water (250°C/4 MPa). Under the hydrothermal conditions of deuterium oxide, decarbonylative deuteration was observed to give fully deuterated hydrocarbons from carboxylic acids or aldehydes.
