4212-04-8 Usage
Chemical compound
A substance formed by the chemical combination of two or more elements in a fixed proportion.
Radical scavenger
A substance that can neutralize free radicals, which are molecules with unpaired electrons that can cause damage to cells and contribute to aging and disease.
Antioxidant
A substance that can prevent or slow down the oxidation process, which can lead to cell damage and the formation of free radicals.
Derivative of N-hydroxyimide
A compound that is structurally related to N-hydroxyimide, a type of organic compound.
Inhibits oxidation process
The compound can slow down or prevent the oxidation process, which can lead to the formation of free radicals and cell damage.
Contains two benzylsulfanyl groups
The compound has two benzylsulfanyl groups attached to its propan-2-imine backbone, which contribute to its chemical structure and properties.
N-hydroxy group
The compound has an N-hydroxy group, which provides its antioxidant properties.
Pharmaceutical and chemical industries
The compound is commonly used in these industries for its free radical scavenging abilities.
Potential applications
The compound has potential applications in the development of antioxidant medications and as a stabilizing agent in various chemical processes.
Antioxidant properties
The compound has antioxidant properties, which can help prevent or slow down the oxidation process and the formation of free radicals.
Industrial applications
The compound has potential industrial applications, such as in the development of antioxidant medications and as a stabilizing agent in chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 4212-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,1 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4212-04:
(6*4)+(5*2)+(4*1)+(3*2)+(2*0)+(1*4)=48
48 % 10 = 8
So 4212-04-8 is a valid CAS Registry Number.
4212-04-8Relevant articles and documents
SYNTHESIS AND PROPERTIES OF N-SUBSTITUTED 4-AMINO-1,2-DITHIOLANES AND RELATED COMPOUNDS
Povalyaeva, O.S.,Rodionov, V.Ya.,Suvorov, N.M.
, p. 773 - 782 (2007/10/02)
Various methods for the synthesis of 4-acylamino-1,2-dithiolanes through N-substituted 1,3-di(benzylthio)-2-propylamines, which exhibit appreciable nematocidal activity, were studied.The 4-methylamino- and 4-amino-1,2-dithiolanes are extremely unstable.On the basis of a study of the electronic absorption spectra it was suggested that these compounds may undergo polymerization to linear polydisulfides at elevated temperatures.
