30860-31-2 Usage
Uses
Used in Biological Studies:
CARBON DISULFIDE (13C) is used as a neurotoxicological indicator for evaluating the toxicity of substances to the brain. It aids in monitoring the effects of potential neurotoxicants through the analysis of EEG readings, providing valuable insights into the impact of these substances on brain function and overall health.
Used in Pharmaceutical Research:
In the field of pharmaceutical research, CARBON DISULFIDE (13C) can be employed as a tracer molecule to study the metabolic pathways and interactions of various drugs and compounds within the body. This information can be instrumental in the development of new drugs and therapies, as well as in understanding the mechanisms of action and potential side effects of existing medications.
Used in Environmental Monitoring:
CARBON DISULFIDE (13C) can also be utilized in environmental monitoring and assessment, where it can help identify and quantify the presence of specific pollutants or contaminants in air, water, or soil samples. This information is crucial for understanding the impact of human activities on the environment and for developing strategies to mitigate or prevent further pollution.
Used in Chemical Synthesis:
In the chemical industry, CARBON DISULFIDE (13C) can be used as a starting material or a reagent in the synthesis of various organic compounds. Its isotopic composition makes it a valuable tool for studying reaction mechanisms and for the production of isotopically labeled compounds, which can be used in a wide range of applications, from research to medical diagnostics.
Used in Material Science:
CARBON DISULFIDE (13C) can also find applications in material science, where it can be used to study the properties and behavior of various materials at the molecular level. This information can be used to develop new materials with improved properties or to optimize the performance of existing materials in various applications, such as electronics, energy storage, and structural components.
Check Digit Verification of cas no
The CAS Registry Mumber 30860-31-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,8,6 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 30860-31:
(7*3)+(6*0)+(5*8)+(4*6)+(3*0)+(2*3)+(1*1)=92
92 % 10 = 2
So 30860-31-2 is a valid CAS Registry Number.
30860-31-2Relevant academic research and scientific papers
Steric and electronic effects in the formation and carbon disulfide reactivity of dinuclear nickel complexes supported by bis(iminopyridine) ligands
Bheemaraju, Amarnath,Beattie, Jeffrey W.,Tabasan, Erwyn G.,Martin, Philip D.,Lord, Richard L.,Groysman, Stanislav
, p. 2952 - 2962 (2013/06/27)
We are developing bimetallic platforms for the cooperative activation of heteroallenes. Toward this goal, we designed a new family of bis(iminopyridine) ((N,N′-1,1′-(1,4-phenylene)bis(N-(pyridin-2-ylmethylene)methanamine) and N,N′-1,1′-(1,4-phenylene)bis(N-(1-(pyridin-2-yl)ethylidene) methanamine)) dinickel complexes, synthesized their CS2 compounds, and studied their reactivity. Bis(iminopyridine) ligands L react with Ni(COD)2 to form Ni2(L)2 complexes or Ni 2(L)(COD)2 complexes as a function of the steric and electronic properties of the ligand precursor. Product structures disclosed an anti geometry in the Ni2(L)(COD)2 species and helical (anti) structures for Ni2(L)2 complexes. Carbon disulfide adducts Ni2(L)(CS2)2 were obtained in good yields upon addition of CS2 to Ni2(L)(COD)2 or in a one-pot reaction of L with 2 equiv of both Ni(COD)2 and CS 2. Ni2(L)(CS2)2 complexes are highly flexible, displaying both syn and anti conformations (shortest S- - -S separations of 5.0 and 9.5 A, respectively) in the solid state. DFT calculations demonstrate virtually no energy difference between the two conformations. Electrochemical studies of the Ni2(L)(CS 2)2 complexes displayed two ligand-based reductions and a broad CS2-based oxidation. Chemical oxidation with [FeCp 2]+ liberated free CS2. The addition of NHC (NHC = 1,3-di-tert-butylimidazolin-2-ylidene) to Ni2(L)(CS 2)2 yielded Ni2(NHC)2(CS 2)2, in which both carbon disulfide ligands are bridging two Ni centers.
The generation and vibrational spectrum of matrix isolated thioformaldehyde and dideuterothioformaldehyde
Torres, M.,Safarik, I.,Clement, A.,Strausz, O. P.
, p. 1187 - 1191 (2007/10/02)
The photolysis of inert matrix isolated methylene trithiocarbonate at 10 K has been shown to be a clean source of thioformaldehyde.The CH2S and CD2S molecules produced this way are indefinitely stable under these conditions and their FTIR spectra could be recorded.A normal coordinate analysis has been carried out and all the normal frequencies of both molecules have been assigned.
