65562-19-8 Usage
Uses
Used in Pharmaceutical Applications:
(5Z)-5-[(4-nitrophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential pharmaceutical compound for its possible biological activity. The presence of the nitrophenyl group and the thiazolidine ring may contribute to its potential use in the development of new drugs.
Used in Medicinal Chemistry Research:
As a complex molecule with a unique structure, (5Z)-5-[(4-nitrophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a research tool in the field of medicinal chemistry. It may be employed to study the interactions between biological molecules and potential drug candidates, contributing to the advancement of drug discovery and development.
Used in Chemical Intermediate Applications:
Due to its complex structure and functional groups, (5Z)-5-[(4-nitrophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one can be used as a chemical intermediate in the synthesis of other compounds. Its versatility in chemical reactions may allow for the creation of new molecules with specific properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-19-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,6 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65562-19:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*1)+(1*9)=138
138 % 10 = 8
So 65562-19-8 is a valid CAS Registry Number.
65562-19-8Relevant academic research and scientific papers
N glucopyranosyl 5 aralkylidenerhodanines: Synthesis and antibacterial and antiviral activities
Foye,Tovivich
, p. 1607 - 1611 (2007/10/08)
A series of N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-aralkylidenerhodanines was synthesized, and the acetyl groups were removed to give N-β-D-glucopyranosyl-5-aralkylidenerhodanines without cleavage of the rhodanine ring by means of acid hydrolysis. Alkaline hydrolysis with ammonia in methanol resulted in cleavage to N-glucosylthiourea, providing evidence for N-glycoside formation. A number of the rhodanine derivatives, especially those with nitro or chloro groups in the aromatic ring, showed antibacterial activity. N-β-D-Glucopyranosyl-5-(4-nitrobenzylidene)rhodanine showed antiviral activity by inhibition of viral RNA synthesis. Some effect on blood sugar levels also was observed with several rhodanines.
