66086-39-3 Usage
Tetrathiocine derivative
A class of organic compounds containing four sulfur atoms in a heterocyclic ring This defines the structure and type of the compound.
Yellow crystalline solid
The physical appearance of the compound, which is a yellow crystalline solid.
Insoluble in water and most organic solvents
The compound does not dissolve easily in water or most organic solvents, which may affect its handling and application.
Potential use as a photoinitiator
2,8-Dimethyldibenzo[c,g][1,2,5,6]tetrathiocine has been studied for its potential use in initiating polymerization reactions upon exposure to light.
Biological activity
The compound has shown potential as an antitumor and antimicrobial agent, which could lead to its use in medical applications.
Promising candidate for various applications
Due to its structure and properties, 2,8-Dimethyldibenzo[c,g][1,2,5,6]tetrathiocine is a candidate for further exploration in industrial and biomedical applications.
Check Digit Verification of cas no
The CAS Registry Mumber 66086-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,8 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66086-39:
(7*6)+(6*6)+(5*0)+(4*8)+(3*6)+(2*3)+(1*9)=143
143 % 10 = 3
So 66086-39-3 is a valid CAS Registry Number.
66086-39-3Relevant articles and documents
Reaction of 2-phenyl-4-(ethoxymethylene)-5(4H)-oxazolone with 3,4-dithio-toluene in the presence of Lewis base
Tikdari, Ahmad Momeni,Hamidian, Hooshang,Razee, Saeid
, p. 2821 - 2826 (2007/10/03)
A convenient procedure for the synthesis of thiocoumarin by the condensation of 2-phenyl-4-(ethoxymethylene)-5-(4H)-oxazolone with 3,4-dithio-toluene in the presence of triethylamine is reported. Here, both thio groups are able to react with the carbonyl group to produce a mixture of isomeric products at ambient temperature. Only one of the isomers upon heating gives a new coumarin product.
Organic chemistry of superoxide. I. Oxidations of aromatic compounds.
Crank,Makin
, p. 2169 - 2170 (2007/10/05)
Potassium superoxide is a selective oxidant for aromatic compounds with the order of susceptibility of substituent groups being -SH>-NH2-OH. Only o- and p- disubstituted amines and phenols are oxidized but monosubstituted thiols react.
