115104-40-0 Usage
General Description
1-(3-(7-Chloro-2-Quinolinyl) Ethyl) is a chemical compound with the molecular formula C15H13ClN2. It is a chloroquinoline derivative, which is a class of chemical compounds that have been found to have various pharmacological properties. Chloroquinolines are commonly used as antimalarial agents, with the ability to inhibit the growth of the malaria parasite in the blood. They are also being researched for their potential use in treating other diseases, such as cancer and autoimmune disorders. The specific properties and applications of 1-(3-(7-Chloro-2-Quinolinyl) Ethyl) are still being studied, but it is a compound of interest for its potential therapeutic applications.
Check Digit Verification of cas no
The CAS Registry Mumber 115104-40-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,1,0 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115104-40:
(8*1)+(7*1)+(6*5)+(5*1)+(4*0)+(3*4)+(2*4)+(1*0)=70
70 % 10 = 0
So 115104-40-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H12ClNO/c19-16-7-5-15-6-9-17(20-18(15)11-16)8-4-13-2-1-3-14(10-13)12-21/h1-12H
115104-40-0Relevant articles and documents
Synthesis, biological evaluations and computational studies of N-(3-(-2-(7-Chloroquinolin-2-yl)vinyl) benzylidene)anilines as fungal biofilm inhibitors
Khan, Firoz A. Kalam,Kaduskar, Rashmi N.,Patil, Rajesh,Patil, Rajendra H.,Ansari, Siddique Akber,Alkahtani, Hamad M.,Almehizia, Abdulrahman A.,Shinde, Devanand B.,Sangshetti, Jaiprakash N.
, p. 623 - 630 (2019)
In the present investigation, new chloroquinoline derivatives bearing vinyl benzylidene aniline substituents at 2nd position were synthesized and screed for biofilm inhibitory, antifungal and antibacterial activity. The result of biofilm inhibition of C.
Process for unsymmetrical dithioacetals and dithioketals
-
, (2008/06/13)
This invention relates to a novel process for preparing unsymmetrical dithioacetals and dithioketals from aryl aldehydes and ketones.
