14397-59-2 Usage
Description
ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) is an isotopically labeled research compound that is utilized in various scientific studies and applications due to its unique properties. It is characterized by its stable isotopic composition, which allows for accurate tracking and analysis in different experimental setups.
Uses
Used in Research and Development:
ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) is used as a research compound for the development and optimization of various chemical processes and reactions. Its isotopically labeled nature enables researchers to study the behavior of the compound in different environments and under various conditions, providing valuable insights into its properties and potential applications.
Used in Analytical Chemistry:
In the field of analytical chemistry, ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) serves as a valuable tool for the identification and quantification of specific compounds. Its unique isotopic signature allows for accurate detection and measurement, making it an essential component in various analytical techniques such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy.
Used in Pharmaceutical Industry:
ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) is used as a compound in the pharmaceutical industry for the synthesis of various drugs and drug candidates. Its unique properties and reactivity make it a versatile building block in the development of new medications, potentially leading to the discovery of novel therapeutic agents.
Used in Environmental Studies:
In environmental science, ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) can be employed as a tracer compound to study the fate and transport of pollutants in the environment. Its isotopically labeled nature allows for the tracking of specific contaminants and their interactions with various environmental matrices, providing valuable information for the assessment and management of environmental risks.
Used in Material Science:
ISOPHORONE (3-METHYL-D3, 2,4,4,6,6-D5) is used as a component in the development of new materials with specific properties. Its unique chemical structure and reactivity can be exploited to create novel materials with enhanced performance characteristics, such as improved mechanical strength, thermal stability, or chemical resistance, for various applications in industries such as automotive, aerospace, and electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 14397-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,9 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14397-59:
(7*1)+(6*4)+(5*3)+(4*9)+(3*7)+(2*5)+(1*9)=122
122 % 10 = 2
So 14397-59-2 is a valid CAS Registry Number.
14397-59-2Relevant articles and documents
Reactions d'addition nucleophiles sur les cetones. Mise en evidence d'un effet directionnel d'origine sterique dans l'effet isotopique secondaire du deuterium
Boyer, Bernard,Lamaty, Gerard,Roque, Jean-Pierre,Geneste, Patrick
, p. 55 - 59 (2007/10/02)
A kinetic study of the addition reactions of borohydride and sulfite ions and of hydroxylamine to a number of stereospecifically deuterated carbonyl compounds (3,3,5,5-tetramethyl cyclohexanone, 7,7-d2-bicyclo-2-norbornanone) leads to the observation of a distant secondary deuterium isotope effect.The results obtained reveal the intervention of a directional effect in the steric origin of these isotope effects.In particular, this study shows the importance of the orientation of the vibrations brought into play by a C-D bond during the reaction process.
