5934-37-2 Usage
Description
(3E)-5-(4-chlorophenyl)-3-[(5-iodofuran-2-yl)methylidene]furan-2(3H)-one is a heterocyclic furan derivative characterized by a furan ring with a 4-chlorophenyl group and a 5-iodofuran-2-yl)methylidene side chain. This unique molecular structure endows it with potential biological activities, making it a molecule of interest for pharmaceutical and medicinal chemistry research.
Used in Pharmaceutical Industry:
(3E)-5-(4-chlorophenyl)-3-[(5-iodofuran-2-yl)methylidene]furan-2(3H)-one is used as a pharmaceutical compound for its potential antiviral, antifungal, and anti-inflammatory properties. Its molecular structure and functional groups contribute to its pharmacological effects, making it a promising candidate for drug development and further investigation in medicinal chemistry research.
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.
