598-16-3 Usage
Uses
Used in Organic Synthesis:
Tribromoethylene is utilized as a solvent for organic materials due to its solubility in organic solvents, facilitating various chemical reactions and processes in the field of organic synthesis.
Used in Agriculture as a Fumigant:
In the agricultural industry, Tribromoethylene serves as a fumigant for stored grains and seeds, helping to protect them from pests and spoilage, thereby ensuring the quality and safety of food supplies.
Used in Pharmaceutical Synthesis:
Tribromoethylene is employed in the synthesis of pharmaceuticals, where it acts as an intermediate in the production of various medicinal compounds, contributing to the development of new drugs and therapies.
Used in Chemical Production:
As an intermediate in the production of other chemicals, Tribromoethylene plays a crucial role in the chemical industry, enabling the creation of a wide range of products used in various applications.
However, it is important to note that Tribromoethylene is classified as a hazardous substance with potential health effects such as eye and skin irritation. It is also considered a potential carcinogen, which necessitates careful handling and use in compliance with safety regulations to minimize exposure and risk.
Check Digit Verification of cas no
The CAS Registry Mumber 598-16-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,9 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 598-16:
(5*5)+(4*9)+(3*8)+(2*1)+(1*6)=93
93 % 10 = 3
So 598-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C2HBr3/c3-1-2(4)5/h1H
598-16-3Relevant academic research and scientific papers
Liquid-phase oxidation of bromovinyl compounds with molecular oxygen
Bayatyan,Bayatyan,Saakyan
, p. 1849 - 1852 (2008/02/08)
Liquid-phase oxidation of bromovinyl compounds with the aim to obtain the corresponding α-bromo acids was studied.
Preparation, reactions, and spectroscopic investigation of the 1,1,3,3-tetramethylimidazolidinium and 1,1,4,4-tetramethylpiperazonium dications
Creighton, J. Alain,Taylor, Michael J.
, p. 2526 - 2528 (2007/10/02)
The title dictations are prepared in a single step by the reaction of N,N,N',N'-tetramethyl-1,2-diaminoethane (tmen) with the halogenoalkanes CH2X2 (X = Cl, Br, or I) or CH2XCH2X (X = Cl or Br), respectively.These bulky dications are useful for the precipitation of complex ions from solution, and show selectivity for doubly-charged anions.Tmen also reacts with CBr4 to yield a dibromo-imidazolidinium heterocyclic dication, whereas reaction with CHBr2CHBr2 produces the dihydrobromide of tmen.Vibration and nmr spectra are reported, and the protons of the CH2 group between the two quaternary nitrogen atoms of the tetramethylimidazolidinium dication are shown from the nmr data to possess acidic character.
