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2,4-dinitro-1-(2-nitrophenoxy)benzene is a chemical compound characterized by a molecular formula of C12H7N3O8. It is a yellow crystalline solid that is widely recognized for its applications in various industries, including organic synthesis, dye and pigment production, and the manufacturing of explosives and propellants. Due to its explosive properties and potential toxicity, it is essential to handle 2,4-dinitro-1-(2-nitrophenoxy)benzene with care to prevent harm to individuals and the environment.

2363-39-5

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2363-39-5 Usage

Uses

Used in Organic Synthesis:
2,4-dinitro-1-(2-nitrophenoxy)benzene is utilized as a reagent in organic synthesis, serving as a key intermediate for the production of various chemical compounds. Its unique structure allows for the creation of a range of products, making it a valuable component in the field of chemistry.
Used in Dye and Pigment Production:
In the dye and pigment industry, 2,4-dinitro-1-(2-nitrophenoxy)benzene is employed as an intermediate, contributing to the development of a diverse array of colorants. Its role in this process is crucial for the production of high-quality dyes and pigments that are used in various applications, such as textiles, plastics, and paints.
Used in Explosive Manufacturing:
2,4-dinitro-1-(2-nitrophenoxy)benzene is known for its explosive properties, making it a critical component in the manufacturing of explosives and propellants. Its ability to release energy rapidly upon initiation is harnessed in the production of these materials, which are used in various applications, such as mining, construction, and military operations.
Used in Propellant Production:
In addition to its use in explosives, 2,4-dinitro-1-(2-nitrophenoxy)benzene is also utilized in the production of propellants. These materials are essential for the propulsion of various devices, such as rockets, missiles, and firearms, and the compound's properties make it a suitable choice for this purpose.
Environmental Considerations:
Due to its toxic nature and potential environmental impact, 2,4-dinitro-1-(2-nitrophenoxy)benzene is classified as a known environmental pollutant. It is crucial to handle and dispose of 2,4-dinitro-1-(2-nitrophenoxy)benzene properly to minimize its effects on ecosystems and human health. This includes taking precautions to prevent ingestion, inhalation, and skin and eye irritation, as well as implementing proper disposal methods to reduce its presence in the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 2363-39-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2363-39:
(6*2)+(5*3)+(4*6)+(3*3)+(2*3)+(1*9)=75
75 % 10 = 5
So 2363-39-5 is a valid CAS Registry Number.

2363-39-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dinitro-1-(2-nitrophenoxy)benzene

1.2 Other means of identification

Product number -
Other names (2,4-dinitro-phenyl)-(2-nitro-phenyl)-ether

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:2363-39-5 SDS

2363-39-5Relevant academic research and scientific papers

The Reduction of Some 2,2'-Dinitrodiaryl Compounds and Related Compounds by Thiourea S,S-Dioxide (Formamidinesulfinic Acid)

Wilshire, John F. K.

, p. 995 - 1001 (2007/10/02)

The reaction of thiourea S,S-dioxide (formamidinesulfinic acid) in ethanolic alkali with 2,2'-dinitrobiphenyl and several related dinitro compounds possessing an-X-bridge (where X = NH, NMe, O and S), located at the 1,1'-positions, has been investigated.With 2,2'-dinitrobiphenyl (which gives good yields of benzocinnoline and its oxides) and, to a minor extent, with 2,2'-dinitrodiphenylamine, an intramolecular reaction occured to give heterocyclic products; with each of the other dinitro compounds, the only product obtained was formed as the result of a Smiles rearrangement.

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