5934-37-2 Usage
General Description
The chemical compound (3E)-5-(4-chlorophenyl)-3-[(5-iodofuran-2-yl)methylidene]furan-2(3H)-one is a furan derivative with a unique molecular structure consisting of a furan ring substituted with a 4-chlorophenyl group and a 5-iodofuran-2-yl)methylidene side chain. It is classified as a heterocyclic compound and is used in pharmaceutical and medicinal chemistry research due to its potential biological activities. (3E)-5-(4-chlorophenyl)-3-[(5-iodofuran-2-yl)methylidene]furan-2(3H)-one may exhibit various pharmacological properties such as antiviral, antifungal, and anti-inflammatory effects. Its structure and functional groups make it a molecule of interest for further investigation and possible drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 5934-37-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5934-37:
(6*5)+(5*9)+(4*3)+(3*4)+(2*3)+(1*7)=112
112 % 10 = 2
So 5934-37-2 is a valid CAS Registry Number.
5934-37-2Relevant articles and documents
Keten. Part 17. Addition Reactions of Ketens with N-Phenyl Nitrones
Hafiz, Mushtag,Taylor, Giles A.
, p. 1700 - 1705 (2007/10/02)
The N-phenyl nitrones (1a), (4b), and (15) react with ketens in two totally different ways.Triphenylnitrone (4b) forms oxidolones (6) whereas (1a) and (15) form oxazolidinones (2) and (17).The differences appear to be caused by steric interactions in (1a) and (15) which distort the nitrone function and prevent the N-phenyl group adopting the conformation necessary for the oxindole-forming pathway.
