128944-81-0 Usage
Uses
Used in Organic Synthesis:
(4Z,5E)-1-[4-(dimethylamino)phenyl]-3-(4-methoxyphenyl)-4,5-bis[(4-methoxyphenyl)imino]imidazolidine-2-thione is used as a key intermediate in the synthesis of various complex organic compounds due to its unique structure and functional groups.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4Z,5E)-1-[4-(dimethylamino)phenyl]-3-(4-methoxyphenyl)-4,5-bis[(4-methoxyphenyl)imino]imidazolidine-2-thione may be utilized as a building block for the development of novel pharmaceuticals, targeting specific biological receptors or enzymes.
Used in Material Science:
(4Z,5E)-1-[4-(dimethylamino)phenyl]-3-(4-methoxyphenyl)-4,5-bis[(4-methoxyphenyl)imino]imidazolidine-2-thione could also find applications in material science, potentially contributing to the development of new materials with unique properties, such as improved conductivity or enhanced stability.
Check Digit Verification of cas no
The CAS Registry Mumber 128944-81-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,4 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128944-81:
(8*1)+(7*2)+(6*8)+(5*9)+(4*4)+(3*4)+(2*8)+(1*1)=160
160 % 10 = 0
So 128944-81-0 is a valid CAS Registry Number.
128944-81-0Relevant articles and documents
On the Reaction of Oxalic Amidines with Carbonic Acid Derived Heterocumulenes to Imidazolidine-Derivatives
Beckert, R.,Gruner, M.
, p. 65 - 82 (2007/10/02)
A useful synthetic route to nonsymmetric derivatives of imidazolidine (derivatives of parabanic acid) is demonstrated by the reaction of tetraarylated oxalic amidines 1 with different alkyl- and aryl substituted isothiocyanates 4, isoselenocyanates 31, and carbodiimides 30.Acylisothiocyanates 9 react differently leading to a mixture of three cycloacylation products 12, 13 and 14.Silylated heterocumulenes such as 25 and 26 react with 1 to give 28 and 29 transsilylation.Based on the 13C-n.m.r. spectroscopic investigation of the reaction between 1a and methyl isothiocyanate and phenyl isothiocyanate respectively a mechanism is proposed.