39091-64-0 Usage
Description
2-IODOPROPANE-1,1,1,3,3,3-D6, with the CAS number 39091-64-0, is an isotopically labeled research compound that is utilized in various scientific studies and experiments. It is a deuterated version of 2-iodopropane, which means it contains deuterium atoms instead of regular hydrogen atoms. This characteristic makes it a valuable tool for researchers to investigate the properties and behavior of molecules in different environments.
Uses
Used in Research and Development:
2-IODOPROPANE-1,1,1,3,3,3-D6 is used as an isotopically labeled compound for research purposes. The deuterium labeling allows researchers to study the effects of isotopic substitution on the compound's chemical and physical properties, as well as its interactions with other molecules. This information can be crucial for understanding the underlying mechanisms of various chemical reactions and processes.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-IODOPROPANE-1,1,1,3,3,3-D6 is used as a research tool for the development of new drugs and therapies. The isotopically labeled compound can be employed to investigate the metabolic pathways and pharmacokinetics of drug candidates, providing valuable insights into their efficacy and safety profiles.
Used in Chemical Industry:
The chemical industry utilizes 2-IODOPROPANE-1,1,1,3,3,3-D6 as a starting material or intermediate in the synthesis of various organic compounds. The deuterium labeling can help in tracing the reaction pathways and understanding the reaction mechanisms, which can be beneficial for optimizing the synthesis processes and improving the overall yield of the desired products.
Used in Environmental Studies:
2-IODOPROPANE-1,1,1,3,3,3-D6 can be employed in environmental studies to investigate the fate and transport of pollutants in the environment. The deuterium labeling allows for the differentiation between naturally occurring and anthropogenic sources of the compound, providing valuable information for assessing the impact of human activities on the environment.
Used in Analytical Chemistry:
In analytical chemistry, 2-IODOPROPANE-1,1,1,3,3,3-D6 is used as an internal standard or reference material for the quantification and identification of target compounds. The deuterium labeling provides a unique signature that can be easily distinguished from the background signals, improving the accuracy and precision of the analytical measurements.
Check Digit Verification of cas no
The CAS Registry Mumber 39091-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,0,9 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 39091-64:
(7*3)+(6*9)+(5*0)+(4*9)+(3*1)+(2*6)+(1*4)=130
130 % 10 = 0
So 39091-64-0 is a valid CAS Registry Number.
39091-64-0Relevant articles and documents
Generation and Trapping of Bis(dialkylamino)silylenes: Experimental Evidence for Bridged Structure of Diaminosilylene Dimers
Sakamoto, Kenkichi,Tsutsui, Shinobu,Sakurai, Hideki,Kira, Mitsuo
, p. 253 - 260 (2007/10/03)
Reduction of dichlorobis(diisopropylamino)silane and dichlorobis(cis-2,6-dimethylpiperidino) silane by alkali metals gave the corresponding bis(diisopropylamino)silylene and bis(cis-2,6-dimethylpiperidino)silylene, respectively. These were successfully trapped by toluene and benzene as well as by hydrosilane, olefin, and acetylene. As the first evidence for the existence of the bridged-dimer of the diaminosilylenes, we have found scrambling of the amino-substituents on a silicon atom during the simultaneous generation of two different bis(dialkylamino)silylenes in benzene. Diaminosilyenes generated thermally from the other new precursors designed here gave no evidence for the bridged dimer, due to the high temperature required for the generation.
Unimolecular Reactions of Ionised 4-Methoxyheptane
Bowen, Richard D.,Derrick, Peter J.
, p. 1041 - 1047 (2007/10/02)
The dissociation of metastable ionised 4-methoxyheptane has been examined by means of extensive 2H-labelling experiments.Only two significant fragmentations are observed, corresponding to loss of ether methanol or propane.Each of these processes involves a hydrogen transfer step in which a pronounced site-selectivity is observed.However, the site-selectivities found for the two fragmentations are distinctly different.Expulsion of methanol, which is characterised by a rather small kinetic energy release, takes place after a unidirectional 1,4-hydrogen transfer to oxygen has occurred; this step is subject to a very large isotope effect.In contrast, loss of propane involves ejection of an intact propyl group, together with an α-hydrogen atom from the second propyl group, via a formal 1,2-elimination.Primary and secondary isotope effects of comparable magnitudes intervene in propane loss from ionised methoxyheptanes in which either or both propyl groups carry 2H-labels on the α-carbon atom.The possibility that ion-neutral complexes are important in the reactions of those C8H18-nDnO+. species is discussed.
