65562-27-8 Usage
General Description
The chemical compound "(5Z)-5-[(4-chlorophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one" is a thiazolidinone derivative with a substituted acetylhexopyranosyl group. It has a thioxo group and a thiazolidinone ring structure. The compound also contains a 4-chlorophenylmethylidene group. Thiazolidinones are known for their potential pharmaceutical properties, including anti-inflammatory, antidiabetic, and antimicrobial activities. The specific structure of this compound suggests potential applications in drug development and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 65562-27-8 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, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65562-27:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*7)=138
138 % 10 = 8
So 65562-27-8 is a valid CAS Registry Number.
65562-27-8Relevant 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.