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2587-01-1

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2587-01-1 Usage

Description

2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE, also known as 2,6-Dichloro-4-nitropyridine-1-oxide (CAS# 2587-01-1), is an organic compound characterized by its yellow powder appearance. It is primarily recognized for its utility in various organic synthesis processes, making it a valuable component in the field of chemistry.

Uses

Used in Organic Synthesis:
2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE is used as a synthetic building block for the creation of various organic compounds. Its unique chemical structure allows it to participate in multiple chemical reactions, facilitating the synthesis of a wide range of molecules with different applications across various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE is used as an intermediate in the development of new drugs. Its reactivity and structural properties make it a suitable candidate for the synthesis of active pharmaceutical ingredients, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Research:
2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE is also utilized in academic and industrial research settings. It serves as a model compound for studying various chemical reactions and mechanisms, contributing to the advancement of knowledge in organic chemistry and related fields.
Used in Agrochemicals:
In the agrochemical sector, 2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE is employed as a starting material for the synthesis of various pesticides and other agricultural chemicals. Its role in this industry is crucial for the development of effective solutions to protect crops and enhance agricultural productivity.
Overall, 2,6-DICHLORO-4-NITROPYRIDINE-N-OXIDE is a versatile compound with a wide range of applications across different industries, primarily due to its utility in organic synthesis and its potential for use in the development of new pharmaceuticals, agrochemicals, and other chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 2587-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2587-01:
(6*2)+(5*5)+(4*8)+(3*7)+(2*0)+(1*1)=91
91 % 10 = 1
So 2587-01-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H2Cl2N2O3/c6-4-1-3(9(11)12)2-5(7)8(4)10/h1-2H

2587-01-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H26979)  2,6-Dichloro-4-nitropyridine N-oxide, 97%   

  • 2587-01-1

  • 5g

  • 508.0CNY

  • Detail
  • Aldrich

  • (673161)  2,6-Dichloro-4-nitropyridineN-oxide  97%

  • 2587-01-1

  • 673161-5G

  • 497.25CNY

  • Detail

2587-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dichloro-4-nitro-1-oxidopyridin-1-ium

1.2 Other means of identification

Product number -
Other names 2,6-Dichlor-4-nitropyridin-1-oxid

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:2587-01-1 SDS

2587-01-1Relevant articles and documents

Efficient synthesis of 4-amino-2,6-dichloropyridine and its derivatives

Ma, Congming,Liu, Zuliang,Yao, Qizheng

, p. 251 - 254 (2016/10/24)

A facile synthetic route to an important intermediate 4-amino-2,6-dichloropyridine was developed. Oxidation of 2,6-dichloropyridine as a starting material gave pyridine N-oxide derivative which was subjected to nitration followed by reduction. Subsequent nitration of the product and nucleophilic displacement reaction were carried out to afford fully substituted energetic pyridine derivatives. Most of the synthetic reactions proceeded under mild conditions.

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