62559-22-2 Usage
Uses
Used in Cancer Treatment:
[dichloro(2-chloroethyl)-lambda~4~-selanyl]benzene is used as a potential therapeutic agent for cancer treatment due to its promising anti-cancer properties. It has been studied for its potential role in inhibiting the growth of cancer cells.
Used in Immune System Modulation:
[dichloro(2-chloroethyl)-lambda~4~-selanyl]benzene is used as an immune system modulator for its ability to modulate the immune system and reduce inflammation.
Used in Inflammation Reduction:
[dichloro(2-chloroethyl)-lambda~4~-selanyl]benzene is used as an anti-inflammatory agent for its ability to reduce inflammation.
Used in Biological Research:
[dichloro(2-chloroethyl)-lambda~4~-selanyl]benzene is used as a research compound in the field of biological research to study its potential applications and mechanisms of action in medical and therapeutic contexts.
Check Digit Verification of cas no
The CAS Registry Mumber 62559-22-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,5,5 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62559-22:
(7*6)+(6*2)+(5*5)+(4*5)+(3*9)+(2*2)+(1*2)=132
132 % 10 = 2
So 62559-22-2 is a valid CAS Registry Number.
62559-22-2Relevant academic research and scientific papers
NUCLEOPHILIC DISPLACEMENT REACTIONS AT Se(II). REACTION OF ARENESELENENYL CHLORIDES AND 2-CHLOROALKYL PHENYL SELENIDES
Schmid, George H.,Garratt, Dennis G.
, p. 4787 - 4792 (2007/10/02)
The products of the title reaction depend upon the relative concentrations of reactants.With equimolar concentrations or an excess of 2-chloroalkyl phenyl selenide, the products are 1,2-dichloroethane and a diaryldiselenide.When excess areneselenenyl chloride is used, the products are a diaryl diselenide and 2-chloroalkyl phenyl selenide dichloride.A mechanism involving nucleophilic displacement at selenenyl selenium is proposed to account for the observed products.Structural changes in the selenide on varying substituents in the 4-position of areneselenenyl chloride has little effect on the rate of the reaction.In the proposed continuum of mechanisms of nucleophilic displacement reactions at Se(II), an SN2-like transition state best accounts for the data.
