24588-56-5 Usage
Uses
Used in Research and Development:
2-Heptanone-1,1,1,3,3-D5 is used as an isotopically labeled compound for research and development purposes. The incorporation of deuterium atoms into the molecule allows for the study of reaction mechanisms, kinetics, and the behavior of the compound in various chemical and biological processes. This is particularly useful in understanding the fundamental aspects of chemical reactions and the role of hydrogen bonding in these processes.
Used in Analytical Chemistry:
In the field of analytical chemistry, 2-Heptanone-1,1,1,3,3-D5 is used as a reference material or internal standard for the accurate quantification and identification of related compounds. The presence of deuterium atoms provides a distinct mass difference, which can be easily detected and utilized for the precise measurement of the target analyte.
Used in Pharmaceutical Industry:
2-Heptanone-1,1,1,3,3-D5 can be employed in the pharmaceutical industry as a tool for studying drug metabolism and pharmacokinetics. The deuterated compound can be used to investigate the metabolic pathways of similar molecules, potentially leading to the development of more effective drugs with improved pharmacological properties.
Used in Environmental Science:
In environmental science, 2-Heptanone-1,1,1,3,3-D5 can be utilized to study the fate and transport of organic compounds in the environment. The deuterated compound can be used as a tracer to track the movement and degradation of related compounds in various environmental matrices, such as soil, water, and air.
Used in Material Science:
2-Heptanone-1,1,1,3,3-D5 can also be employed in material science research, particularly in the study of polymers and their interactions with other molecules. The deuterated compound can provide insights into the molecular dynamics and structural properties of polymers, which can be crucial for the development of new materials with specific characteristics and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 24588-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,5,8 and 8 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 24588-56:
(7*2)+(6*4)+(5*5)+(4*8)+(3*8)+(2*5)+(1*6)=135
135 % 10 = 5
So 24588-56-5 is a valid CAS Registry Number.
24588-56-5Relevant academic research and scientific papers
Aerobic oxidation of alkenes mediated by porphyrin rhodium(iii) complexes in water
Zhang, Jiadi,Li, Shan,Fu, Xuefeng,Wayland, Bradford B.
scheme or table, p. 3661 - 3663 (2009/08/15)
Selective oxidation of alkenes in water to ketones using molecular oxygen as the oxidant is mediated by rhodium porphyrin complexes through observed β-hydroxy alkyl complexes.
Deuterium Nuclear Magnetic Resonance Study of Solid Deoxycholic Acid Adducts: Structure, Dynamics, and Photochemical Reactivity
Meirovitch, Eva
, p. 2385 - 2393 (2007/10/02)
We report cn an 2H NMR study of polycrystalline powders of several deoxycholic acid (DOCA) inclusion compounds between 150 and 350 K.The information obtained relates primarily to the conformation, flexibility, and mobility of the quest molecules, their intrachannel orientation and site multiplicity, and the effect of a photochemical guest-host reaction on these characteristics.With acetophenone, fluoroacetophenone, acetic acid, p- and o-xylene, and acetone rapid internal methyl rotation persist at all temperatures investigated.The C-CD3 bonds were found to fluctuate about a mean orientation within the channel.The amplitude of these fluctuations was found to be side specific, temperature dependent, and suppressible upon cooling and following occurence of the guest-host reaction.Ring inversion was observed with tetrahydrofuran (THF), cyclohexane, and cyclohexanone.Discrete jumps about symmetry axes of the guest molecule or the host lattice were detected with acetophenone and o-xylene, the flip motion taking place between unequally populated sites.In some cases, such as the cyclohexane and acetic acid adducts, there are sites in the host lattice where, on the average, the guest molecules reorient isotropically.
