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3-Methoxy-4-nitropyridine N-oxide is a chemical compound characterized by the molecular formula C6H6N2O4. It presents as a white to yellow powder and is recognized for its role in the synthesis of pharmaceutical compounds and organic dyes. 3-Methoxy-4-nitropyridine N-oxide also serves as an intermediate in chemical reactions and is utilized as a research reagent in various scientific laboratories. Due to its potential hazards if ingested, inhaled, or absorbed through the skin, it is crucial to handle 3-Methoxy-4-nitropyridine N-oxide with care and adhere to safety guidelines. Moreover, proper storage and disposal are essential to prevent environmental contamination.

19355-04-5

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19355-04-5 Usage

Uses

Used in Pharmaceutical Industry:
3-Methoxy-4-nitropyridine N-oxide is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure allows it to be a building block for the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Organic Dyes Industry:
In the realm of organic dyes, 3-Methoxy-4-nitropyridine N-oxide is employed as a precursor for the production of dyes with specific color properties. Its chemical composition plays a vital role in determining the hue and stability of the resulting dyes, making it an important component in the dye manufacturing process.
Used in Chemical Research:
3-Methoxy-4-nitropyridine N-oxide is utilized as a research reagent in laboratories, where it aids in the investigation of chemical reactions and the development of new synthetic pathways. Its presence in experiments can provide insights into reaction mechanisms and the properties of various chemical systems.
Used in Chemical Reactions as an Intermediate:
3-Methoxy-4-nitropyridine N-oxide is used as an intermediate in a variety of chemical reactions, facilitating the synthesis of complex organic molecules. Its reactivity and functional groups make it a versatile component in organic synthesis, enabling the creation of a wide range of compounds for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 19355-04-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,5 and 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19355-04:
(7*1)+(6*9)+(5*3)+(4*5)+(3*5)+(2*0)+(1*4)=115
115 % 10 = 5
So 19355-04-5 is a valid CAS Registry Number.

19355-04-5SDS

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 3-methoxy-4-nitro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names N-oxide of 3-methoxy-4-nitropyridine

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:19355-04-5 SDS

19355-04-5Relevant academic research and scientific papers

COMPOUNDS AND COMPOSITIONS FOR TREATING CONDITIONS ASSOCIATED WITH STING ACTIVITY

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Page/Page column 125, (2022/01/24)

The present invention relates to chemical entities (for example, a pharmaceutically acceptable compound or salt, and / or a hydrate, and / or a co-crystal, and / or a combination of drug of the compound) which inhibit (for example, antagonize) the stimula

Heterocyclic compound used as MNK inhibitor

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, (2019/01/08)

The invention relates to a heterocyclic compound, a pharmaceutical composition containing the heterocyclic compound, a preparation method thereof, and application thereof used as a mitogen activated protein kinase interacting kinase 1 and 2-MNK1/MNK2 inhibitor. The inhibitor is the heterocyclic compound as shown in the formula (I), or its pharmaceutically acceptable salt, prodrug, solvent compound, polycrystal, isomer, stable isotope derivative or a pharmaceutical composition containing the heterocyclic compound. The compound of the invention can be used for treating or preventing MNK-mediatedrelated diseases, such as cancers.

PEST CONTROL AGENT

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Paragraph 0136, (2016/10/09)

PROBLEM TO BE SOLVED: To provide a compound having high activity to pest, a pest control agent obtained using the compound and a method for controlling pest by application of the compound. SOLUTION: The present invention provides the pest control agent co

SMALL MOLECULE AGONISTS OF NEUROTENSIN RECEPTOR 1

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, (2016/04/26)

Provided herein are small molecule neurotensin receptor agonists, compositions comprising the compounds, and methods of using the compounds and compositions comprising the compounds.

PEST CONTROL AGENT

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Page/Page column 40, (2014/07/08)

Objects of the present invention are to provide a compound which is highly active against pests, to provide a pest control agent comprising the compound, and to provide a method for controlling a pest by applying the compound. The present invention provid

Hydrogen bonding-mediated self-assembly of square and triangular metallocyclophanes

Wu, Zong-Quan,Jiang, Xi-Kui,Li, Zhan-Ting

, p. 8067 - 8070 (2007/10/03)

Intramolecular three-centered hydrogen bonding has been used to induce dipyridyl anthranilamide 5 and diphenylacetylene anthranilamide 11 to adopt rigid straight conformation. Compound 5 reacted with Pd(dppp)(OTf)2 (12a) or Pt(dppp)(OTf)2 (12b) in dichloromethane to afford square metallocyclophanes 13a and 13b in 70% and 40% yield, respectively. In contrast, the reaction of 11 with 12b in dichloromethane gave triangular metallocyclophane 14 in 15% yield.

A USEFUL CONSTRUCTION OF 4-SUBSTITUTED 1-ALKYLPIPERID-3-ONES

Swindell, Charles S.,Duffy, Ruth H.

, p. 3373 - 3377 (2007/10/02)

A potentially general construction of 4-substituted 1-alkylpiperid-3-ones is described which employs 3-methoxy-4-bromopyridine as the crucial reagent.This substance is coupled at C-4 with Grignard reagents through the Kumada reaction.The resulting pyridines are then N-alkylated and subsequently subjected to borohydride reduction and aqueous acidic hydrolysis to reveal the title piperidones and related substances.

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