847020-99-9 Usage
Molecular structure
The compound has an isoindole-1,3(2H)-dione ring structure with a 2-[3-[4-oxo-2-(phenylimino)-3-thiazolidinyl]propoxy] side chain attached.
Thiazolidinyl group
The compound contains a thiazolidinyl group (a five-membered ring with two nitrogen atoms and one sulfur atom) which may contribute to its potential medicinal properties.
Phenylimino group
The presence of a phenylimino group (a phenyl ring connected to a nitrogen atom via a double bond) can influence the compound's biological activities and therapeutic applications.
Keto group
The compound features a keto group (a carbonyl functional group with a double bond between the carbon and oxygen atoms) which can affect its reactivity and interactions with other molecules.
Potential medicinal properties
The compound exhibits potential medicinal properties, making it relevant in drug design and development.
Structural and chemical characteristics
It is essential to consider the compound's structural and chemical characteristics in the context of its potential biological activities and therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 847020-99-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,0,2 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 847020-99:
(8*8)+(7*4)+(6*7)+(5*0)+(4*2)+(3*0)+(2*9)+(1*9)=169
169 % 10 = 9
So 847020-99-9 is a valid CAS Registry Number.
847020-99-9Relevant academic research and scientific papers
Synthesis and biological evaluation of 7-N-(n-alkoxyphthalimido)-2hydroxy- 4-aryl-6-aryliminothiazolidino [2,3-b] pyrimidines and related compounds
Singh, Bhawani Singh,Mehta, Deepika,Baregama, Lalit K.,Talesara
, p. 1306 - 1313 (2007/10/03)
Substituted aryl thioureas 1a-c react with chloroacetic acid in the presence of anhydrous sodium acetate to furnish 2-aryliminothiazolidin-4-ones 2a-c. Condensation of ω-bromoalkoxyphthalimides 3a-c with 2a-c give the corresponding alkoxyphthalimide derivatives of 2-aryliminothiazolidin-4-ones 4a-i. These on condensation with araldehydes 5a-c yield 3-N-(alkoxyphthalimido)- 5-arylidene-2-aryliminothiazolidin-4-ones 7a-a′. In an alternative route 5a-c react with 2a-c to give 6a-i, which could be cyclised with urea in the presence of sodium acetate to yield the corresponding thiazolidinopyrimidine 8a-i. 7a-a′ are also prepared from 6a-i with 3a-c, which give final compound 9a-a′ on cyclisation. Alternatively, 8a-i when condensed with 3a-c also furnish the compounds 9a-a′. Evaluation of antimalarial and antibacterial activity is also reported.
