497084-47-6 Usage
General Description
3-Iodoquinolin-8-amine is a chemical compound classified under the category of quinolines and isoquinolines. It's known for its dense molecular structure with a molecular weight of 309.053 g per mol. 3-IODOQUINOLIN-8-AMINE has a diverse set of applications in chemical and biomedical research due to its unique properties.The unique properties and structure of this compound make it useful in the development of pharmaceuticals and as an important precursor in organic synthesis. Details regarding its safety, toxicity, and handling precautions have to be taken into account before usage. As with all chemical substances, its interaction with other compounds and its impact on the environment must be thoroughly recognized and evaluated.
Check Digit Verification of cas no
The CAS Registry Mumber 497084-47-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,7,0,8 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 497084-47:
(8*4)+(7*9)+(6*7)+(5*0)+(4*8)+(3*4)+(2*4)+(1*7)=196
196 % 10 = 6
So 497084-47-6 is a valid CAS Registry Number.
497084-47-6Relevant articles and documents
Effect of 3-subsitution of quinolinehydroxamic acids on selectivity of histone deacetylase isoforms
Mehndiratta, Samir,Chen, Mei-Chuan,Chao, Yuh-Hsuan,Lee, Cheng-Hsin,Liou, Jing-Ping,Lai, Mei-Jung,Lee, Hsueh-Yun
, p. 74 - 84 (2020/11/10)
A series of 3-subsituted quinolinehydroxamic acids has been synthesised and evaluated for their effect on human lung cancer cell line (A549), human colorectal cancer cell line (HCT116) and HDAC isoforms 1, 2, 6, and 8. The results indicated that substitut
Preparation and antifungal activity of 3-Iodo- and 6-Iodo-8-quinolinols
Gershon, Herman,Clarke, Donald D.,McMahon, John J.,Gershon, Muriel
, p. 1325 - 1330 (2007/10/03)
3-Iodo- and 6-Iodo-8-quinolinols were prepared and tested against six fungi: Aspergillus niger, A. oryzae, Myrothecium verrucaria, Trichoderma viride, Mucor cirinelloides, and Trichophyton mentagrophytes in Sabouraud dextrose broth. A comparison with the previously known 5-iodo- and 7-iodo-8-quinolinols showed that the 6-iodo isomer was the most active.
