65562-41-6 Usage
Uses
Used in Pharmaceutical Industry:
(5Z)-5-(naphthalen-2-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential drug candidate for its diverse pharmacological activities, including antibacterial, antiviral, antitumor, and anti-inflammatory properties. (5Z)-5-(naphthalen-2-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's unique structure and functional groups contribute to its potential therapeutic applications.
Used in Drug Development Research:
(5Z)-5-(naphthalen-2-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a subject of study in drug development research to understand its pharmacological potential and biological effects. The presence of the thiazolidin-4-one ring and the naphthalene group, along with the acetylated hexopyranosyl moiety, makes it an interesting molecule for further investigation into its possible uses in medicine.
Used in Chemical Synthesis:
(5Z)-5-(naphthalen-2-ylmethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one may also be used in chemical synthesis as a starting material or intermediate for the creation of other complex organic molecules with potential applications in various fields, including pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-41-6 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, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 65562-41:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*4)+(1*1)=136
136 % 10 = 6
So 65562-41-6 is a valid CAS Registry Number.
65562-41-6Relevant 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.
