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10-Oxylatoacridine-10-ium is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10399-73-2

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10399-73-2 Usage

Chemical compound

OAA is a chemical compound with potential anti-cancer properties.

Family

It belongs to the acridine family of compounds.

Cationic species

OAA is a cationic species, meaning it has a positive charge.

Anti-cancer effects

OAA has been studied for its ability to inhibit the growth of cancer cells.

Cancer types

It has shown potential in treating melanoma and breast cancer.

Mechanism of action

OAA is believed to exert its anti-cancer effects by inducing DNA damage and interfering with DNA repair processes.

Photosensitizer

OAA has shown promise as a photosensitizer for photodynamic therapy.

Photodynamic therapy

This treatment uses light to activate a photosensitizing agent, such as OAA, to destroy cancer cells.

Ongoing research

Research on OAA is ongoing to better understand its potential and develop new anti-cancer therapies.

Development of therapies

The ultimate goal of the research is to harness the potential of OAA for the development of new and effective anti-cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 10399-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10399-73:
(7*1)+(6*0)+(5*3)+(4*9)+(3*9)+(2*7)+(1*3)=102
102 % 10 = 2
So 10399-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H

10399-73-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-oxidoacridin-10-ium

1.2 Other means of identification

Product number -
Other names Acridine,10-oxide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:10399-73-2 SDS

10399-73-2Upstream product

10399-73-2Relevant academic research and scientific papers

Influence of a reaction medium on the oxidation of aromatic nitrogen-containing compounds by peroxyacids

Dutka,Matsyuk,Dutka

, p. 45 - 50 (2011)

The influence of different solvents on the oxidation reaction rate of pyridine (Py), quinoline (QN), acridine (AN), α-oxyquinoline (OQN) and a-picolinic acid (APA) by peroxydecanoic acid (PDA) was studied. It was found that the oxidation rate grows in the series Py eq) and its decomposition constant (k2) in acetone and benzene were calculated. It was shown that the nature of the solvent influences the numerical values of both Kp and k2. It was established that introduction of acetic acid (which is able to form compounds with Py) into the reaction medium slows the rate of the oxidation process drastically. Correlation equations linking the polarity, polarizability, electrophilicity, and basicity of solvents with the constant of the PDA oxidation reaction rate for Py were found. It was concluded that the basicity and polarity of the solvent have a decisive influence on the oxidation reaction rate, while the polarizability and electrophilicity of the reaction medium do not influence the oxidation reaction rate. Pleiades Publishing, Ltd., 2011.

KINETICS OF N-OXIDATION OF COMPOUNDS OF THE QUINOLINE SERIES AND ISOMERIC BENZOQUINOLINES BY PERBENZOIC ACID IN CHLOROFORM AND AQUEOUS DIOXANE

Lokhov, R. E.

, p. 72 - 76 (1981)

The kinetics of the N-oxidation with perbenzoic acid of 15 derivatives of quinoline and benzoquinoline in chloroform and 19 compounds in 50percent aqueous dioxane at 20, 25, 30, and 35 deg C were subjected to a comparative study.The rate constants, parameters of Arrhenius equation, and the activation energies for the N-oxidation of the indicated monoazines were determined.A scale of the reactivities of derivatives of the quinoline series and benzoquinolines was calculated within the framework of general perturbation theory.

Co(III)-Catalyzed C-H Amidation of Nitrogen-Containing Heterocycles with Dioxazolones under Mild Conditions

Dhiman, Ankit Kumar,Thakur, Ankita,Kumar, Inder,Kumar, Rakesh,Sharma, Upendra

, p. 9244 - 9254 (2020)

A cobalt(III)-catalyzed C-8 selective C-H amidation of quinoline N-oxide using dioxazolone as an amidating reagent under mild conditions is disclosed. The reaction proceeds efficiently with excellent functional group compatibility. The utility of the current method is demonstrated by gram scale synthesis of C-8 amide quinoline N-oxide and by converting this amidated product into functionalized quinolines. Furthermore, the developed catalytic method is also applicable for C-7 amidation of N-pyrimidylindolines and ortho-amidation of benzamides.

Formation of the N-oxides of heteroaromatic nitrogen compounds by perfluorinated oxaziridines

Balsarini, Christian,Novo, Barbara,Resnati, Giuseppe

, p. 31 - 34 (1996)

On treatment with perfluoro-cis-2,3-dialkyloxaziridines, mono-, bi-, and tricyclic nitrogen heteroaromatics afford the corresponding N-oxides under mild reaction conditions and in medium to high yields. The course of the reaction is not altered by the presence of various residues on the ring or in side chains and the N-oxides of polyfunctional, naturally occurring compounds have been prepared.

Effects of Supramolecular Architecture on Halogen Bonding between Diiodine and Heteroaromatic N-Oxides

Nizhnik, Yakov P.,Sons, Alex,Zeller, Matthias,Rosokha, Sergiy V.

, p. 1198 - 1207 (2018)

Cocrystallization of diiodine with a series of heteroaromatic N-oxides produced three types of halogen-bonded associates: (a) alternating chains comprising I2 molecules bridged by oxygen atoms of N-oxides of pyridine, quinoline, or 4-methylpyridine; (b) discrete 2:1 complexes, in which diiodine links a pair of acridine N-oxide molecules; and (c) amphoteric 1:1 adducts, in which one end of each diiodine molecule is halogen-bonded to N-oxide of 4-methoxypyridine or 4-chloroquinoline, and another diiodine's end forms contacts with the other I2 molecules. In all cases, halogen bonds between diiodine and N-oxides are characterized by nearly linear I-I···O angles, close to perpendicular dihedral C-N-O···I angles and N-O···I angles of about 110°. The halogen bond length in the 1:1 adducts is about 0.3 ? shorter than those in the 2:1 associates and in the infinite chains. Computational analyses confirmed that the variations in I···O separations are related predominantly to the distinct effects of halogen bond competition in different supramolecular associates. Experimental and computational data also indicated that coordination of the second diiodine to the same oxygen atom of N-oxide has a smaller effect on the halogen bond length and energy than coordination of the second N-oxide to another iodine atom in the I2 molecule.

Ru-Catalyzed Deoxygenative Regioselective C8-H Arylation of Quinoline N-Oxides

Kim, Jinwoo,Kim, Suhyeon,Kim, Dongwook,Chang, Sukbok

, p. 13150 - 13158 (2019/08/22)

Regioselective C-H functionalization on quinolines is of high interest to lead to value-added products. Herein, we describe the development of Ru-catalyzed deoxygenative regioselective C8 arylation of quinoline N-oxides with arylboronic esters. Mechanistic studies revealed that it proceeds in a tandem process of arylation and then deoxygenation, wherein both steps were found to be catalytic with the ruthenium species.

Strategic Approach on N-Oxides in Gold Catalysis – A Case Study

Schie?l, Jasmin,Stein, Philipp M.,Stirn, Judith,Emler, Kirsten,Rudolph, Matthias,Rominger, Frank,Hashmi, A. Stephen K.

supporting information, p. 725 - 738 (2018/10/20)

An extensive kinetic study of selected key reactions of (oxidative) gold catalysis concentrates on the decrease of the catalytic activity due to inhibition of the gold(I) catalyst caused by pyridine derivatives that are obtained as by-products if N-oxides are applied as oxygen donors. The choice of the examined pyridine derivatives and their corresponding N-oxides has been made regardless of their commercial availability; particular attention has been paid to the practical benefit which up to now has been neglected in most of the reaction screenings. The test reactions were monitored by GC and 1H NMR spectroscopy. The received reaction constants provide information concerning a correlation between the electronic structure of the heterocycle and the catalytic activity. Based on the collected kinetic data, it was possible to develop a basic set of three N-oxides which have to be taken into account in further oxidative gold(I)-catalyzed reactions. (Figure presented.).

RhIII-Catalyzed Straightforward Synthesis of Benzophenanthroline and Benzophenanthrolinone Derivatives using Anthranils

Biswas, Aniruddha,Sarkar, Souradip,Samanta, Rajarshi

, p. 3000 - 3004 (2019/02/13)

An efficient pot-economic and step-economic RhIII-catalyzed site-selective direct amination/annulation strategy was developed for the synthesis of benzophenanthroline derivatives using quinoline N-oxides and anthranils. The method was further extended to the synthesis of nitrogen-containing extended π-conjugated benzophenanthrolinone derivatives. Late-stage functionalizations of cinchonidine and cinchophen derivatives and synthesis of a bioactive quinolino-indole were achieved.

Regioselective Cyanation of Six-Membered N-Heteroaromatic Compounds Under Metal-, Activator-, Base- and Solvent-Free Conditions

Sarmah, Bikash Kumar,Konwar, Monuranjan,Bhattacharyya, Dipanjan,Adhikari, Priyanka,Das, Animesh

supporting information, p. 5616 - 5625 (2019/11/22)

A regioselective cyanation of heteroaromatic N-oxides with trimethylsilyl cyanide has been developed to obtain 2-substituted N-heteroaromatic nitrile without the requirement of any external activator-, metal-, base-, and solvent. The present protocol is a straightforward, one-pot heteroaromatic C?H cyanation process, and proceeds smoothly in conventional heating but also under microwave irradiation with shorter reaction times. This approach now allows access to a broad class of quinoline N-oxides and other heteroarene N-oxides with high to good yields and can also be scaled up to obtain gram quantities. Further application of this process was observed and utilized in late-stage cyanation of the anti-malarial drug quinine as well as transformation of the 2-cyanoazines to a series of biologically important molecules. Based on the experimental observations, a plausible mechanism has also been proposed highlighting the dual role of trimethylsilyl cyanide as a nitrile source and as an activating agent. (Figure presented.).

Electrochemical Deoxygenation of N-Heteroaromatic N -Oxides

Xu, H.-C.,Xu, P.

supporting information, p. 1219 - 1221 (2019/06/08)

An electrochemical method for the deoxygenation of N-heteroaromatic N -oxide to give the corresponding N-heteroaromatics has been developed. Several classes of N-heterocycles such as pyridine, quinoline, isoquinoline, and phenanthridine are tolerated. The electrochemical reactions proceed efficiently in aqueous solution without the need for transition-metal catalysts and waste-generating reducing reagents.

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