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2,3-Dimethylpyridine-d9, with the CAS number 350818-65-4, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a derivative of pyridine, an important heterocyclic compound, with two methyl groups attached at the 2nd and 3rd positions and a deuterium atom (D9) replacing nine hydrogen atoms. This stable isotope labeling allows for enhanced detection and tracing of the compound in complex biological systems.

350818-65-4

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350818-65-4 Usage

Uses

Used in Chemical Research:
2,3-Dimethylpyridine-d9 is used as a labeled compound for chemical research, particularly in the study of reaction mechanisms, metabolic pathways, and the synthesis of various organic compounds. The presence of deuterium atoms in the molecule provides a unique signature that can be easily distinguished from its non-labeled counterpart, facilitating the tracking of chemical transformations and the identification of reaction intermediates.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,3-Dimethylpyridine-d9 is used as a labeled compound for drug discovery and development. It can be employed as a reference material for the identification and quantification of active pharmaceutical ingredients, as well as for the study of drug metabolism and pharmacokinetics. The stable isotope labeling aids in the differentiation of the compound from endogenous substances, providing more accurate and reliable data in pharmacological studies.
Used in Environmental Research:
2,3-Dimethylpyridine-d9 is also used as a labeled compound in environmental research, where it can help in understanding the fate and transport of pollutants in the environment. The stable isotope labeling allows for the tracking of the compound in complex environmental matrices, such as soil, water, and air, providing valuable insights into the behavior of pollutants and their potential impact on ecosystems.
Used in Analytical Chemistry:
In analytical chemistry, 2,3-Dimethylpyridine-d9 serves as a valuable internal standard or reference material for the quantification and identification of target analytes. The stable isotope labeling ensures accurate measurement and comparison of the compound's concentration in various samples, improving the reliability and precision of analytical results.
Used in Material Science:
2,3-Dimethylpyridine-d9 can be employed in material science research, where it may be used to study the interactions between different materials or to develop new materials with specific properties. The stable isotope labeling can help in understanding the molecular-level processes involved in material formation and degradation, contributing to the development of advanced materials with improved performance characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 350818-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,0,8,1 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 350818-65:
(8*3)+(7*5)+(6*0)+(5*8)+(4*1)+(3*8)+(2*6)+(1*5)=144
144 % 10 = 4
So 350818-65-4 is a valid CAS Registry Number.

350818-65-4Upstream product

350818-65-4Downstream Products

350818-65-4Relevant academic research and scientific papers

METHOD FOR DEUTERATION OR TRITIATION OF HETEROCYCLIC RING

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Page/Page column 20-21, (2008/06/13)

The present invention relates to a method for deuteration of a heterocyclic ring, which comprises subjecting a compound having a heterocyclic ring to sealed refluxing state in a deuterated solvent in the presence of an activated catalyst selected form a palladium catalyst, a platinum catalyst, a rhodium catalyst, a ruthenium catalyst, a nickel catalyst and a cobalt catalyst. In accordance with a method of the present invention, a hydrogen atom belonging to a heterocyclic ring of a compound having a heterocyclic ring can be very efficiently deuterated because temperature of deuteration reaction can be maintained at higher than boiling point of the solvent. Further, a method for deuteration of the present invention can be applied widely to deuteration of various compounds having a heterocyclic ring which are liable to decomposition under supercritical conditions or acidic conditions, leading to industrial and efficient deuteration of a compound having a heterocyclic ring.

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