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2-(3,4-dichlorophenoxy)-5-nitropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25935-29-9

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25935-29-9 Usage

Nitro-substituted pyridine derivative

A compound derived from pyridine (a five-membered aromatic ring with six valence electrons) by substituting a nitro group (-NO2) on the pyridine ring.

Chlorine atoms

Two chlorine atoms are attached to the phenoxy ring, which can influence the compound's reactivity, stability, and solubility.

Nitro group

A nitro group (-NO2) is attached to the pyridine ring, which can affect the compound's chemical properties and reactivity.

Phenoxy ring

A phenol (a benzene ring with a hydroxyl group) is attached to the pyridine ring through an ether linkage (-O-), which can influence the compound's reactivity and stability.

Intermediate in synthesis

2-(3,4-dichlorophenoxy)-5-nitropyridine is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds, meaning it is a reactant in the production of these compounds.

Building block in fine chemicals production

The compound serves as a building block in the production of a wide range of fine chemicals, which are high-value, specialized chemical products used in various industries.

Potential applications in materials science and chemical research

Due to its unique structure and reactivity, 2-(3,4-dichlorophenoxy)-5-nitropyridine has potential applications in the development of new materials and the study of chemical reactions and processes.

Potential toxicity and harmful effects

The compound may have toxic and harmful effects on human health and the environment, so it should be handled and used with caution.

Appropriate laboratory settings

2-(3,4-dichlorophenoxy)-5-nitropyridine should be handled and used in controlled laboratory environments with proper safety measures and equipment to minimize the risk of exposure and harm.

Check Digit Verification of cas no

The CAS Registry Mumber 25935-29-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,3 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25935-29:
(7*2)+(6*5)+(5*9)+(4*3)+(3*5)+(2*2)+(1*9)=129
129 % 10 = 9
So 25935-29-9 is a valid CAS Registry Number.

25935-29-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4-dichlorophenoxy)-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-(3,4-dichloro-phenoxy)-5-nitro-pyridine

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:25935-29-9 SDS

25935-29-9Relevant academic research and scientific papers

Antipicornavirus activity of substituted phenoxybenzenes and phenoxypyridines

Markley,Tong,Dulworth,Steward,Goralski,Johnston,Wood,Vinogradoff,Bargar

, p. 427 - 433 (2007/10/02)

Phenoxybenzenes and phenoxypyridines were prepared and tested for the effect of substituents on antipicornavirus activity. The most active compound, 2-(3,4-dichlorophenoxy)-5-nitrobenzonitrile (8), demonstrated broad-spectrum antipicornavirus activity. Co

Sulfur-substituted phenoxypyridines having antiviral activity

-

, (2008/06/13)

Sulfur-substituted phenoxypyridines having antiviral activity are disclosed. Methods of using the sulfur-substituted phenoxypyridines to employ their antiviral activity are also disclosed as well as pharmaceutically-acceptable compositions thereof.

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