{"references": ["[1]\tCollin G, Hoke H, Ullman, Willey-VCH Weinheim, 22 (2005) 465.", "[2]\tKannappan N, Reddy B S R, Sen S, Nagarajan R, Dashpute S, Journal of Applied Chemical Research, 9 (2009) 59-68.", "[3]\tU S Environmental Protection Agency (U.S.EPA), Federal Register, 61(79) (1996) 17960-18011.", "[4]\tU.S. Environmental Protection Agency (U.S.EPA). (1985)", "[5]\tWorld Malaria Report 2008 World Health Organization, Geneva, 2008", "[6]\tKumar MMJ, Yogananda R, Snehalatha Shameer H, Jayachandran E Sreenivasa GMJ, Biomed Sci Res., 1(2009) 1-10.", "[7]\tRamalakshmishmi N and Bharathi RV, Chem Tech., 1 (2009) 1000-1004.", "[8]\tLuoZai-gang, Zeng Cheng-chu, Wang Fang, He Hong-qiu, Wang Cun-xin, Du Hong-guang and Huliming, Chem. Res. Chinese Universities, 25 (6) (2009) 841- 845.", "[9]\tBhandari S V, Deshmane B J, Dangare S C, Gore Sj T, Raparti V T, Khachane C V, Sarkate A P, Pharmacologyonline, 2 (2008) 604-613.", "[10]\tCarlos M, Mel\u00e9ndez G\u00f3mezand, Vladimir V Kouznetsov, (A. M\u00e9ndez-Vilas, Ed.) FORMATEX 2013.", "[11]\tRitu B Dixit, Tarosh S Patel, Satish F Vanparia, Anju P Kunjadiya, Harish R Keharia and Bharat C Dixit, Sci. Pharm.,79 (201) 293-308.", "[12]\tKaur Kirandeep, Jain Meenakshi, Reddy Ravi P, Jain Rahul, European Journal of Medicinal Chemistry, 45 (2010) 3245-3264.", "[13]\tTekwani Babu L, Walker Larry A, Current Opinion in Infectious Diseases, (2006) 19623\u2013631.", "[14]\tDonnell F, Smyth T J P, Ramachandran V N, Smyth W F, International Journal of Antimicrobial Agents, 35 (1) (2009) 3", "[15]\tChintakunta Ramesh, Po-Min Lei, Veerababurao Kavala, Chun-Wei Kuo and Ching-Fa Yao, Molecules, 17 (2012) 5081-5094."]}

Abstract: Quinoline is a hygroscopic liquid that is colorless has a pungent odor and Darkens with age. It is soluble in alcohol, ether, benzene, and carbon disulfide and is sparingly soluble in water. Quinoline is a weak tertiary base. It forms salts in acids and exhibits reactions similar to benzene and pyridine, and can engage in both electrophilic and nucleophilic substitution (HSDB), Quinoline, also known as 1-azanaphthalene, 1-benzazine, or benzo[b]pyridine, is a heterocyclic aromatic organic compound. It has the formula C9H7N. Quinoline structure is known ever since 1908 and proved by total synthesis by Wood ward and Doe ring in 1945. It was the structural model for other anti-malarial quinoline derivatives. It was first isolated by Runge in 1834 from coal tar bases and subsequently, Coal tar remains as the principle source of commercial quinoline; If its aged sample is exposed to light, it turns became yellow and later brown. Keywords: QuinoLine, Pharmaceutical, Heterocyclic. Title: A REVIEW ON QUINOLINE AND ITS DERIVATIVES Author: Jatolia S.N., Shubh laxmi, Kanahiya Lal, Bhojak N, Regar O.P International Journal of Novel Research in Physics Chemistry & Mathematics ISSN 2394-9651 Vol. 9, Issue 2, May 2022 - August 2022 Page No: 6-16 Novelty Journals Website: www.noveltyjournals.com Published Date: 20-June-2022 DOI: https://doi.org/10.5281/zenodo.6670407 Paper Download Link (Source) https://www.noveltyjournals.com/upload/paper/A%20REVIEW%20ON%20QUINOLINE-20062022-4.pdf

International Journal of Novel Research in Physics Chemistry & Mathematics, ISSN 2394-9651, Novelty Journals, Website: www.noveltyjournals.com