114058-79-6 Usage
General Description
7-Quinolinamine, 4-methyl-(9CI) is a chemical compound with the molecular formula C10H9N. It is a derivative of quinoline, a heterocyclic compound with a nitrogen atom in the ring. 7-Quinolinamine,4-methyl-(9CI) is also known as 4-Methylquinolin-7-amine. It is commonly used in the pharmaceutical industry as a starting material for the synthesis of various bioactive molecules and pharmaceutical drugs. It has also been studied for its potential biological activities, including antiviral and antioxidant properties. The compound has a molecular weight of 143.19 g/mol and a boiling point of approximately 342°C. Overall, 7-Quinolinamine, 4-methyl-(9CI) is a versatile chemical with potential applications in drug discovery and development.
Check Digit Verification of cas no
The CAS Registry Mumber 114058-79-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,0,5 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 114058-79:
(8*1)+(7*1)+(6*4)+(5*0)+(4*5)+(3*8)+(2*7)+(1*9)=106
106 % 10 = 6
So 114058-79-6 is a valid CAS Registry Number.
114058-79-6Relevant articles and documents
7-Aminoquinolines. A novel class of agents active against herpesviruses
Nasr,Drach,Smith,Shipman Jr.,Burckhalter
, p. 1347 - 1351 (2007/10/02)
A series of 7-aminoquinoline derivatives was synthesized and evaluated for their capacity to produce cytotoxicity in KB cells and to inhibit the replication of herpes simplex virus (HSV) type 1. All compounds tested inhibited the replication of HSV-1 with 50% inhibitory concentrations in the range of 2-50 μg/mL. The antiviral activity of many compounds, however, was separated from cytotoxicity to replicating uninfected cells by only two- to fivefold higher than those required for antiviral activity. Nonetheless, six compounds (10, 28, 29, 32, 34, and 36) were identified in which the separation was greater than fivefold. All compounds examined were more potent inhibitors of viral DNA synthesis than the cellular DNA synthesis.
