53472-17-6 Usage
Uses
Used in Pharmaceutical Industry:
6-Aminoquinoline hydrochloride is used as an intermediate in the synthesis of various pharmaceuticals for its versatile chemical properties and potential therapeutic applications.
Used in Agrochemical Industry:
6-Aminoquinoline hydrochloride is utilized as an intermediate in the development of agrochemicals, contributing to the creation of effective products for agricultural use.
Used in Anti-malarial Drug Development:
6-Aminoquinoline hydrochloride is used as a key component in anti-malarial drug research and development due to its ability to inhibit the growth of the malaria parasite, offering a potential solution to combat this global health issue.
Used in Photochemical Reactions:
6-Aminoquinoline hydrochloride is employed as a photoreactive material in the study and development of photochemical reactions, expanding its applications in various scientific fields.
Check Digit Verification of cas no
The CAS Registry Mumber 53472-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,4,7 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 53472-17:
(7*5)+(6*3)+(5*4)+(4*7)+(3*2)+(2*1)+(1*7)=116
116 % 10 = 6
So 53472-17-6 is a valid CAS Registry Number.
53472-17-6Relevant academic research and scientific papers
Sch?fberger, Wolfgang,Timelthaler, Daniel,Topf, Christoph
, p. 2114 - 2120 (2021)
We report on the first cobalt corrole that effectively mediates the homogeneous hydrogenation of structurally diverse nitroarenes to afford the corresponding amines. The given catalyst is easily assembled prior to use from 4-tert-butylbenzaldehyde and pyrrole followed by metalation of the resulting corrole macrocycle with cobalt(II) acetate. The thus-prepared complex is self-contained in that the hydrogenation protocol is free from the requirement for adding any auxiliary reagent to elicit the catalytic activity of the applied metal complex. Moreover, a containment system is not required for the assembly of the hydrogenation reaction set-up as both the autoclave and the reaction vessels are readily charged under a regular laboratory atmosphere.
