65562-22-3 Usage
General Description
The chemical "(5Z)-5-(1,3-benzodioxol-5-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one" is a complex compound with multiple functional groups. It contains a benzodioxol ring, an acetate group, a thioxo group, a thiazolidin ring, and a hexopyranosyl group. The presence of these groups suggests that this compound may have potential medicinal or biological properties. The compound's molecular structure, with its various functional groups, could potentially interact with biological targets, making it a potential candidate for drug development or biochemical research. The presence of the thiazolidin-4-one ring also suggests that it may have antidiabetic, anti-inflammatory, or antiviral properties. Overall, this compound's complex structure and functional groups make it an intriguing target for further exploration in the field of medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-22-3 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, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 65562-22:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*2)=133
133 % 10 = 3
So 65562-22-3 is a valid CAS Registry Number.
65562-22-3Relevant articles and documents
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.