3359-52-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
This is an alternative name for the compound, which is used to describe its structure more specifically.
Explanation
The color of the compound when it is in its solid or liquid form.
Explanation
The compound dissolves easily in certain organic solvents but does not dissolve in water.
Explanation
The compound is used to bind and separate metal ions in various chemical and biological processes.
Explanation
The compound is used to remove metal ions from solutions, which can be important in various chemical and industrial processes.
Explanation
The compound is used as a reagent to identify and quantify metal ions present in a solution.
Explanation
The compound has been studied for its potential to help treat cases of metal poisoning by binding to and removing toxic metal ions from the body.
Explanation
The compound has been investigated for its ability to neutralize harmful reactive oxygen species, which can cause cellular damage and contribute to various diseases.
Appearance
Yellowish
Solubility
Soluble in organic solvents (e.g., ethanol, acetone), insoluble in water
Application
Chelating agent in analytical chemistry and biochemical applications
Use in purification
Purification of metal ions
Use as a reagent
Determination of metals in solution
Potential use
Treatment of metal poisoning
Antioxidant properties
Studied for its potential antioxidant effects
Check Digit Verification of cas no
The CAS Registry Mumber 3359-52-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,5 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3359-52:
(6*3)+(5*3)+(4*5)+(3*9)+(2*5)+(1*2)=92
92 % 10 = 2
So 3359-52-2 is a valid CAS Registry Number.
3359-52-2Relevant articles and documents
REACTION OF N-HALOGENOIMIDES WITH SULFUR. THIODIIMIDES
Borovikova, G.S.,Levchenko, E.S.,Kaminskaya, E.I.
, p. 86 - 92 (2007/10/02)
The reaction of N-halogenoimides with sulfur leads to the production of thiodiimides.The latter are active sulfur-transferring reagents.
REACTIONS OF N,N'-DISUBSTITUTED SULFUR DIIMIDES WITH CH ACIDS. II. REACTION OF N,N'-BIS(PHENYLSULFONYL)SULFUR DIIMIDE WITH 5,5-DIMETHYL-1,3-DIOXOCYCLOHEXANE
Levchenko, E. S.,Gaidamaka, S. N.,Kalinin, V. N.,Budnik, L. V.
, p. 871 - 875 (2007/10/02)
The reaction of N,N'-bis(phenylsulfonyl)sulfur diimide with 5,5-dimethyl-1,3-dioxocyclohexane in a ratio of 1:2 leads to the formation of 4-oxo-6,6-dimethyltetrahydro-1,3-benzoxathiole-2-spiro-4',4'-dimethylcyclohexane-2',6'-dione.
