646996-44-3 Usage
Description
6-nitroquinolin-3-amine is an organic compound with the chemical formula C9H7N3O2. It is a derivative of quinoline and contains a nitro group and an amino group on the quinoline ring. This chemical is used in the synthesis of various pharmaceuticals and agrochemicals, and it also has potential applications in organic synthesis and chemical research. 6-nitroquinolin-3-amine is considered to be hazardous and should be handled with care, as it may cause skin and eye irritation and is harmful if swallowed or inhaled. It is important to follow safety precautions when working with this chemical and to dispose of it properly according to regulations.
Uses
Used in Pharmaceutical Industry:
6-nitroquinolin-3-amine is used as an intermediate in the synthesis of various pharmaceuticals for its potential therapeutic properties.
Used in Agrochemical Industry:
6-nitroquinolin-3-amine is used as a building block in the development of agrochemicals to enhance crop protection and yield.
Used in Organic Synthesis:
6-nitroquinolin-3-amine is used as a reagent in organic synthesis processes to create a variety of chemical compounds.
Used in Chemical Research:
6-nitroquinolin-3-amine is used as a research chemical to study its properties and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 646996-44-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,6,9,9 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 646996-44:
(8*6)+(7*4)+(6*6)+(5*9)+(4*9)+(3*6)+(2*4)+(1*4)=223
223 % 10 = 3
So 646996-44-3 is a valid CAS Registry Number.
646996-44-3Relevant articles and documents
Substituted indoloquinolines as new antifungal agents.
Ablordeppey, Seth Y,Fan, Pingchen,Li, Shouming,Clark, Alice M,Hufford, Charles D
, p. 1337 - 1346 (2007/10/03)
Cryptolepine (2) possesses desirable properties to serve as a lead in developing new antifungal agents. Using SAR techniques, several analogues of cryptolepine were designed to increase potency and to broaden the antifungal spectrum over several opportuni
