38470-27-8 Usage
Type of compound
Heterocyclic compound
Structural components
Iodo group, quinolin-4-one moiety
Potential applications
Medicinal chemistry and drug discovery
Reason for potential applications
Structural properties and the presence of an iodo group
Possible uses
Further modifications to develop new pharmaceutical compounds
Current status of research
Specific properties and potential uses are still under investigation
Additional research needed
To fully understand the compound's potential applications in various fields of chemistry and biology
Check Digit Verification of cas no
The CAS Registry Mumber 38470-27-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,4,7 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38470-27:
(7*3)+(6*8)+(5*4)+(4*7)+(3*0)+(2*2)+(1*7)=128
128 % 10 = 8
So 38470-27-8 is a valid CAS Registry Number.
38470-27-8Relevant articles and documents
Synthesis of 2,3-dihydro-4(1H)-quinolones and the corresponding 4(1H)-quinolones via low-temperature fries rearrangement of N-arylazetidin-2- ones
Lange, Jens,Bissember, Alex C.,Banwell, Martin G.,Cade, Ian A.
, p. 454 - 470 (2011/10/09)
N-Arylazetidin-2-ones of the general form 1, which are readily prepared by GoldbergBuchwald-type copper-catalyzed coupling of N-unsubstituted azetidin-2-ones with the relevant aryl halide or using Mitsunobu cyclization processes, undergo smooth Fries-rearrangement in triflic acid at 018°C to give the isomeric 2,3-dihydro-4(1H)-quinolones (2). Dehydrogenation of the latter compounds using 10% Pd on C in 1.0M aqueous sodium hydroxide/propan-2-ol mixtures at ca. 82°C provides the corresponding 4(1H)-quinolones (3).
