142044-38-0 Usage
Description
(+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is a chemical compound that is an epoxide derivative of quinoline N-oxide. It is a white to yellowish solid with a molecular formula of C9H9NO3.
Uses
Used in Organic Synthesis:
(+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is used as a reagent in chemical reactions for organic synthesis, enabling the creation of various complex organic molecules.
Used in Pharmaceutical Compound Preparation:
(+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is used as a building block for the synthesis of novel compounds with potential pharmaceutical applications, contributing to the development of new drugs.
Used in Medicinal Chemistry Research:
(+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is used as a compound with potential anticancer and antimalarial properties, making it valuable in medicinal chemistry research for exploring its therapeutic potential.
Used in Anticancer Applications:
In the field of oncology, (+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is used as a compound with potential anticancer properties, warranting further investigation into its ability to target and treat cancer cells.
Used in Antimalarial Applications:
In the field of infectious diseases, (+-)-cis-5,6-Epoxy-5,6-dihydroquinoline N-oxide is used as a compound with potential antimalarial properties, indicating its possible use in developing treatments for malaria.
Check Digit Verification of cas no
The CAS Registry Mumber 142044-38-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,4 and 4 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142044-38:
(8*1)+(7*4)+(6*2)+(5*0)+(4*4)+(3*4)+(2*3)+(1*8)=90
90 % 10 = 0
So 142044-38-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H7NO2/c11-10-5-1-2-6-7(10)3-4-8-9(6)12-8/h1-5,8-9H/t8-,9+/m1/s1
142044-38-0Relevant articles and documents
Arene Oxides of Quinoline: Epoxidation, N-Oxidation and N-Methylation Reactions
Boyd, Derek R.,Davies, R. Jeremy H.,Hamilton, Lynne,McCullough, John J.,Porter, H. Patricia
, p. 2189 - 2192 (2007/10/02)
trans-5,6,7,8-Diepoxy-5,6,7,8-tetrahydroquinoline 5, 5,6-epoxy-5,6-dihydroquinoline 1-oxide 3, 7,8-epoxy-7,8-dihydroquinoline 1-oxide 4 and trans-5,6,7,8-diepoxy-5,6,7,8-tetrahydroquinoline 6 have been formed by oxidation of the corresponding arene oxides of quinoline, 5,6-epoxy-5,6-dihydroquinoline 1 and 7,8-epoxy-7,8-dihydroquinoline 2.The cis-diepoxides, cis-5,6,7,8-diepoxy-5,6,7,8-tetrahydroquinoline 8 and cis-5,6,7,8-diepoxy-5,6,7,8-tetrahydroquinoline 1-oxide 9 were both obtained by a stepwise synthesis from 7,8-epoxy-7,8-dihydroquinoline 2 via the bromohydrin 7.N-Methylation of 5,6-epoxy-5,6-dihydroquinoline 1 and 7,8-epoxy-7,8-dihydroquinoline 2 with methyl trifluoromethanesulfonate yielded the corresponding N-methylquinolinium arene oxide salts 10 and 11.
