30385-86-5 Usage
Uses
Used in Research and Development:
Ethyl 3-Hydroxy-3-methyl-d3-butyrate--d3 is used as a research compound for various scientific applications. The incorporation of deuterium isotopes in the molecule allows researchers to study the effects of isotopic substitution on the compound's properties and behavior. This can be particularly useful in understanding reaction mechanisms, investigating the role of specific atoms in biological processes, and developing new synthetic methods.
Used in Chemical Synthesis:
In the field of chemical synthesis, Ethyl 3-Hydroxy-3-methyl-d3-butyrate--d3 can be used as a starting material or an intermediate in the preparation of other deuterated compounds. The presence of deuterium isotopes can provide valuable insights into the reaction pathways and help optimize the synthesis process.
Used in Biochemical Studies:
Ethyl 3-Hydroxy-3-methyl-d3-butyrate--d3 can also be employed in biochemical research, where it can serve as a labeled substrate or an inhibitor for enzymes involved in the metabolism of related compounds. The use of deuterated compounds in such studies can help elucidate enzyme mechanisms and provide information on the role of individual atoms in the catalytic process.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Ethyl 3-Hydroxy-3-methyl-d3-butyrate--d3 can be utilized in the development of new drugs and drug candidates. The deuterated compound can be used to study the pharmacokinetics, pharmacodynamics, and metabolic pathways of related drug molecules, which can be crucial in optimizing their efficacy and safety profiles.
Used in Analytical Chemistry:
Ethyl 3-Hydroxy-3-methyl-d3-butyrate--d3 can be employed as an internal standard or a reference compound in various analytical techniques, such as mass spectrometry and nuclear magnetic resonance (NMR) spectroscopy. The use of deuterated compounds as internal standards can improve the accuracy and precision of quantitative measurements, while their unique isotopic signatures can aid in the identification and characterization of complex mixtures.
Check Digit Verification of cas no
The CAS Registry Mumber 30385-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,8 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30385-86:
(7*3)+(6*0)+(5*3)+(4*8)+(3*5)+(2*8)+(1*6)=105
105 % 10 = 5
So 30385-86-5 is a valid CAS Registry Number.
30385-86-5Relevant academic research and scientific papers
Base-initiated Reformatsky Condensations in the Gas Phase
Castle, Lyle W.,Hayes, Roger N.,Gross, Michael L.
, p. 267 - 271 (2007/10/02)
The ester enolate anion CH2=C(OEt)O- reacts with acetaldehyde and with acetone in the gas phase to produce "stable" adducts that are amenable to study by collisional activation and tandem mass spectrometry (MS/MS).The activated adducts and deprotonated β-hydroxy ethyl ester reference ions both decompose by elimination of H2O, Et*, H2O followed by EtOH, and by a retro reaction to reform CH2=C(OEt)O-.The losses of H2O, Et*, and EtOH are assigned to be characteristic of a species of tetrahedral geometry.These losses are, however, attenuated for the ion-molecule adducts because, in addition to existing as tetrahedral complexes, they are also formed as ion-dipole and proton-bound species.
