51592-06-4 Usage
Uses
Used in Radioiodination:
1,3,4,6-TETRACHLORO-3ALPHA,6ALPHA-DI-PHENYLGLYCOURIL is used as an iodination reagent in radioiodination processes, acting as an oxidative agent. Its ability to facilitate the incorporation of radioactive iodine into biomolecules makes it a valuable tool in various research and diagnostic applications.
Used in Comparison Studies:
1,3,4,6-TETRACHLORO-3ALPHA,6ALPHA-DI-PHENYLGLYCOURIL is also utilized as a reagent in comparison studies with chloramine-T, another oxidative agent. By comparing the efficiency and specificity of 1,3,4,6-TETRACHLORO-3ALPHA,6ALPHA-DI-PHENYLGLYCOURIL to that of chloramine-T, researchers can gain insights into the optimal conditions and reagents for specific radioiodination applications.
Used in Oxidation of Urazoles:
1,3,4,6-TETRACHLORO-3ALPHA,6ALPHA-DI-PHENYLGLYCOURIL is employed as a reagent for the oxidation of urazoles, which are heterocyclic compounds with potential applications in various fields, including pharmaceuticals and materials science. 1,3,4,6-TETRACHLORO-3ALPHA,6ALPHA-DI-PHENYLGLYCOURIL's ability to selectively oxidize urazoles makes it a useful tool in the synthesis of novel urazole derivatives with desired properties.
Check Digit Verification of cas no
The CAS Registry Mumber 51592-06-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,9 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 51592-06:
(7*5)+(6*1)+(5*5)+(4*9)+(3*2)+(2*0)+(1*6)=114
114 % 10 = 4
So 51592-06-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H10Cl4N4O2/c17-21-13(25)23(19)16(12-9-5-2-6-10-12)15(21,11-7-3-1-4-8-11)22(18)14(26)24(16)20/h1-10H
51592-06-4Relevant academic research and scientific papers
Improved Halogenation of Methyl Aromatics and Methyl Heteroaromatics: Unexpected Reactivity of Tetrahalogeno-diphenylglycolurils
Moretti, Florian,Poisson, Guillaume,Marsura, Alain
, p. 173 - 183 (2016/05/19)
1,3,4,6-Tetrachloro (TCDGU) and 1,3,4,6-tetrabromo-3α,6α-diphenylglycolurils smooth halogen oxidizers have been exploited in a new direction as reagents for free radical substitution toward some N-halosuccinimide nonreactive bis-heterocycles. An unexpected selectivity and reactivity were observed with methyl benzenes, methyl heterocycles, and methyl-bis-heterocycles of interest. A chemometric study has been performed to optimize five independent factors of the chlorination reaction with TCDGU. The predictive model was established either for the halogenation conversion and the ratio of monochlorination.
Preparation of several active N-chloro compounds from trichloroisocyanuric acid
Shiri, Azam,Khoramabadi-Zad, Ahmad
experimental part, p. 2797 - 2801 (2010/01/21)
A very simple method for the preparation of several activeN-chloro compounds that have extensive applications in organic synthesis, industry, and medicine has been developed.Tetrachloroglycolurils, chloramine-T, N-chlorosaccharin, N-chlorosuccinimide, N-chlorophthalimide, N,N￠-dichlorophenobarbital,and N,N￠-dichlorobarbital were synthesized by chlorination with trichloroisocyanuric acid under mild reaction conditions at roomtemperature. This method is clean, fast, and efficient; the yields are also good to excellent. Georg Thieme Verlag Stuttgart.
