79838-91-8 Usage
Description
(5E)-5-[(4-chlorophenyl)methylidene]-1-(3-methoxyphenyl)-2-sulfanylidene-3-(2,4,6-trimethylphenyl)-1,3-diazinane-4,6-dione is a complex organic molecule characterized by its multiple functional groups and aromatic rings. It features a sulfur atom, a nitrogen atom, and a diazinane ring, which is a six-membered nitrogen heterocycle. The presence of 4-chlorophenyl and 3-methoxyphenyl groups indicates potential pharmacological or biological activity, as these groups are often found in pharmaceutical compounds. Additionally, the 2,4,6-trimethylphenyl group contributes to the compound's complexity, possibly affecting its physical and chemical properties. This versatile molecule could have a range of applications in medicinal chemistry, material science, and other fields.
Uses
Used in Pharmaceutical Industry:
(5E)-5-[(4-chlorophenyl)methylidene]-1-(3-methoxyphenyl)-2-sulfanylidene-3-(2,4,6-trimethylphenyl)-1,3-diazinane-4,6-dione is used as a potential pharmaceutical compound for its possible biological activity. The presence of various functional groups and aromatic rings suggests that it may interact with biological targets, making it a candidate for drug development.
Used in Material Science:
In the field of material science, (5E)-5-[(4-chlorophenyl)methylidene]-1-(3-methoxyphenyl)-2-sulfanylidene-3-(2,4,6-trimethylphenyl)-1,3-diazinane-4,6-dione could be utilized for the development of new materials with specific properties. (5E)-5-[(4-chlorophenyl)methylidene]-1-(3-methoxyphenyl)-2-sulfanylide ne-3-(2,4,6-trimethylphenyl)-1,3-diazinane-4,6-dione's unique structure and functional groups may contribute to the creation of materials with tailored characteristics for various applications.
Used in Chemical Research:
(5E)-5-[(4-chlorophenyl)methylidene]-1-(3-methoxyphenyl)-2-sulfanylidene-3-(2,4,6-trimethylphenyl)-1,3-diazinane-4,6-dione may also be employed in chemical research as a model compound to study the effects of different functional groups and structural features on a molecule's reactivity, stability, and other chemical properties. This could lead to a better understanding of molecular design principles and the development of new synthetic strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 79838-91-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 8 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79838-91:
(7*7)+(6*9)+(5*8)+(4*3)+(3*8)+(2*9)+(1*1)=198
198 % 10 = 8
So 79838-91-8 is a valid CAS Registry Number.
InChI:InChI=1/C27H23ClN2O3S/c1-16-12-17(2)24(18(3)13-16)30-26(32)23(14-19-8-10-20(28)11-9-19)25(31)29(27(30)34)21-6-5-7-22(15-21)33-4/h5-15H,1-4H3/b23-14+
79838-91-8Relevant articles and documents
Compounds Acting on Cardiovascular System: Part III - Synthesis of Some New Thiobarbituric Acid Derivatives
Agarwal, Jagdish C.,Gupta, Y. K.,Bhargava, K. P.,Shanker, K.
, p. 714 - 716 (2007/10/02)
Sixteen new 1-aryl-3-(2',4',6'-trimethylphenyl)-5-(substituted benzylidene)thiobarbituric Acids (III) have been synthesized by the condensation of appropriate aldehydes with 1-aryl-3-(2',4',6'-trimethylphenyl)thiobarbituric acid (II), and evaluated for their cardiovascular activity in anaesthetized dogs.Some of the compounds exhibit promising hypotensive activity of varying magnitude and duration.
