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2-Chloropyridine-N-oxide is an organic compound characterized by its cytotoxic and clastogenic properties. It is a white solid with a molecular structure that includes a chlorine atom attached to the second carbon of the pyridine ring and an oxide group attached to the nitrogen atom. 2-Chloropyridine-N-oxide is known for its potential applications in various fields due to its unique chemical properties.

2402-95-1

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2402-95-1 Usage

Uses

Used in Pharmaceutical Industry:
2-Chloropyridine-N-oxide is used as an intermediate in the synthesis of various pharmaceutical compounds for its cytotoxic and clastogenic properties. These properties make it a valuable component in the development of drugs that target cancer cells by disrupting their replication and division processes.
Used in Chemical Research:
In the field of chemical research, 2-Chloropyridine-N-oxide serves as a key compound for studying the effects of cytotoxic and clastogenic agents on cellular processes. Its unique structure allows researchers to investigate the mechanisms of action and potential applications in targeted therapies.
Used in Material Science:
2-Chloropyridine-N-oxide's chemical properties also make it a candidate for use in material science, particularly in the development of new materials with specific properties. Its cytotoxic nature could be harnessed to create materials with antimicrobial or antifungal properties, for example.

Check Digit Verification of cas no

The CAS Registry Mumber 2402-95-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,0 and 2 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2402-95:
(6*2)+(5*4)+(4*0)+(3*2)+(2*9)+(1*5)=61
61 % 10 = 1
So 2402-95-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H3ClFNO/c6-5-4(7)2-1-3-8(5)9/h1-3H

2402-95-1 Well-known Company Product Price

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  • Alfa Aesar

  • (L20033)  2-Chloropyridine N-oxide, 97%   

  • 2402-95-1

  • 1g

  • 366.0CNY

  • Detail
  • Alfa Aesar

  • (L20033)  2-Chloropyridine N-oxide, 97%   

  • 2402-95-1

  • 5g

  • 1220.0CNY

  • Detail

2402-95-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names N-oxy-2-chlorpyridine

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:2402-95-1 SDS

2402-95-1Relevant academic research and scientific papers

Au(I)-Catalyzed Oxidative Functionalization of Yndiamides

Tong, Zixuan,Garry, Olivia L.,Smith, Philip J.,Jiang, Yubo,Mansfield, Steven J.,Anderson, Edward A.

supporting information, p. 4888 - 4892 (2021/06/28)

Yndiamides, underexplored cousins of ynamides, offer rich synthetic potential as doubly nitrogenated two carbon building blocks. Here we report a gold-catalyzed oxidative functionalization of yndiamides to access unnatural amino acid derivatives, using a wide range of nucleophiles as a source of the amino acid side chain. The transformation proceeds under mild conditions, is highly functional group tolerant, and displays excellent regioselectivity through subtle steric differentiation of the yndiamide nitrogen atom substituents.

From Pyridine- N-oxides to 2-Functionalized Pyridines through Pyridyl Phosphonium Salts: An Umpolung Strategy

Bugaenko, Dmitry I.,Yurovskaya, Marina A.,Karchava, Alexander V.

supporting information, p. 6099 - 6104 (2021/08/03)

The reactions of pyridine-N-oxides with Ph3P under the developed conditions provide an unprecedented route to (pyridine-2-yl)phosphonium salts. Upon activation with DABCO, these salts readily serve as functionalized 2-pyridyl nucleophile equivalents. This umpolung strategy allows for the selective C2 functionalization of the pyridine ring with electrophiles, avoiding the generation and use of unstable organometallic reagents. The protocol operates at ambient temperature and tolerates sensitive functional groups, enabling the synthesis of otherwise challenging compounds.

Recyclable anhydride catalyst for H2O2 oxidation:: N -oxidation of pyridine derivatives

Gajeles, Ghellyn,Kim, Se Mi,Lee, Kyung-Koo,Lee, Sang Hee,Yoo, Jong-Cheol

, p. 9165 - 9171 (2020/03/13)

The catalytic efficiency and recyclability of poly(maleic anhydride-alt-1-octadecene) (Od-MA) and poly(maleic anhydride-alt-1-isobutylene) (Bu-MA) were evaluated for use in the development of a metal-free, reusable catalyst for the oxidation of pyridines to pyridine N-oxides in the presence of H2O2. The Od-MA catalyst was easily recovered via filtration with recovery yields exceeding 99.8%. The catalyst retained its activity after multiple uses and did not require any treatment for reuse. The Od-MA and H2O2 catalytic system described herein is eco-friendly, operationally simple, and cost-effective; thus, it is industrially applicable. Od-MA and H2O2 could potentially be used in place of percarboxylic acid as an oxidant in a wide range of oxidation reactions.

Method for catalyzing vitamin A isomerization with ruthenium catalyst

-

Paragraph 0050; 0053-0054, (2020/04/22)

The invention provides a method for catalyzing vitamin A isomer conversion with a ruthenium catalyst. According to the method, a ruthenium compound is used as a catalyst, various vitamin A cis-isomerswith low biological activity can be converted into all-trans-isomers with high biological activity in a high proportion in the presence of an auxiliary agent, and the cis-isomers comprise 9-cis-isomers, 11-cis-isomers and 13-cis-isomers. The method has the characteristics of cheap and easily available catalyst, less catalyst dosage, mild reaction conditions, low reaction cost, high isomerizationefficiency and the like.

Preparation method of 2-chloro-4-aminopyridine

-

Paragraph 0016; 0019; 0020; 0023; 0024; 0028; 0029, (2020/05/05)

The invention belongs to the field of organic synthesis, and particularly relates to a preparation method of 2-chloro-4-aminopyridine. The preparation method comprises the following steps: (1) using 2-chloropyridine as a raw material and chloroform as a solvent, and generating 2-chloropyridine oxide under the action of m-chloroperoxybenzoic acid; (2) reacting 2-chloropyridine oxide with a mixed acid composed of concentrated nitric acid and concentrated sulfuric acid to generate 2-chloro-4-nitropyridine oxynitride; and (3) reducing 2-chloro-4-nitropyridine oxynitride into 2-chloro-4-aminopyridine. The method has the beneficial effects that the reaction conditions are mild, the operation is easy, the post-treatment is simple, the scale-up production is easy, the method is very suitable for industrial production; the catalytic effect is good, the yield is high; the raw materials are cheap, and the production cost is low.

Visible-Light-Mediated C-H Alkylation of Pyridine Derivatives

Rammal, Fatima,Gao, Di,Boujnah, Sondes,Gaumont, Annie-Claude,Hussein, Aqeel A.,Lakhdar, Sami

supporting information, p. 7671 - 7675 (2020/10/09)

We report herein a visible-light-mediated C-H alkylation of pyridine derivatives that proceeds by simple combination of a large variety of N-alkoxypyridinium ions with alkanes in the presence of 2 mol % of fac-Ir(ppy)3 under blue illumination. The mild reaction conditions together with the high group functional tolerance make of this process a useful synthetic platform for the construction of structurally strained heterocycles. Detailed mechanistic investigations, including density functional theory calculations and quantum yield measurement, allowed us to understand factors controlling the reactivity and the selectivity of the reaction.

Reaction of Pyridine-N-Oxides with Tertiary sp2-N-Nucleophiles: An Efficient Synthesis of Precursors for N-(Pyrid-2-yl)-Substituted N-Heterocyclic Carbenes

Bugaenko, Dmitry I.,Karchava, Alexander V.,Yurovskaya, Marina A.

supporting information, p. 5777 - 5782 (2020/12/01)

N-(Pyrid-2-yl)-substituted azolium and pyridinium salts, precursors for hybrid NHC-containing ligands, were obtained with excellent regioselectivity, employing a deoxygenative CH-functionalization of pyridine-N-oxides with substituted imidazoles, thiazoles, and pyridine. Unlike the traditional SNAr-based methods, this approach provides high yields for substrates bearing substituents of different electronic nature. The utility of azolium and pyridinium salts thus prepared was also highlighted by the synthesis of pyridyl-substituted imidazolyl-2-thione, benzodiazepine as well as 2-aminopyridines.

A 2 - chloro -4 - aminopyridine preparation method

-

Paragraph 0016; 0019; 0020; 0023; 0024; 0028; 0029, (2019/05/28)

The invention belongs to the field of organic synthesis, in particular relates to a 2 - chloro - 4 - aminopyridine preparation method, comprises the following steps: (1) to 2 - chloro pyridine as raw materials, chloroform as solvent, under the action of the meta-chloroperoxybenzoic acid to produce 2 - chloro pyridine oxide; (2) 2 - chloro pyridine oxide by the concentrated nitric acid in concentrated sulfuric acid the acid produced by the reaction of a 2 - chloro - 4 - nitro pyridine nitrogen oxides; (3) 2 - chloro - 4 - nitro pyridine nitrogen oxide reduction is 2 - chloro - 4 - aminopyridine. The beneficial effect of the invention is: mild reaction conditions, is easy to operate, after treatment is simple, and easy to enlarge production, is extremely suitable for industrial production; good catalytic effect, high yield; low prices of raw materials, the production cost is low.

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.).

A Biocatalytic Synthesis of Heteroaromatic N-Oxides by Whole Cells of Escherichia coli Expressing the Multicomponent, Soluble Di-Iron Monooxygenase (SDIMO) PmlABCDEF

Petkevi?ius, Vytautas,Vaitekūnas, Justas,Taurait?, Daiva,Stankevi?iūt?, Jonita,?arlauskas, Jonas,??nas, Narimantas,Me?kys, Rolandas

supporting information, p. 2456 - 2465 (2019/01/25)

Aromatic N-oxides (ArN?OX) are desirable biologically active compounds with a potential for application in pharmacy and agriculture industries. As biocatalysis is making a great impact in organic synthesis, there is still a lack of efficient and convenient enzyme-based techniques for the production of aromatic N-oxides. In this study, a recombinant soluble di-iron monooxygenase (SDIMO) PmlABCDEF overexpressed in Escherichia coli was showed to produce various aromatic N-oxides. Out of 98 tested N-heterocycles, seventy were converted to the corresponding N-oxides without any side oxidation products. This whole-cell biocatalyst showed a high activity towards pyridines, pyrazines, and pyrimidines. It was also capable of oxidizing bulky N-heterocycles with two or even three aromatic rings. Being entirely biocatalytic, our approach provides an environmentally friendly and mild method for the production of aromatic N-oxides avoiding the use of strong oxidants, organometallic catalysts, undesirable solvents, or other environment unfriendly reagents. (Figure presented.).

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