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1,2-Dihydroacenaphthylene-1,3,5-trinitrobenzene (1:1) is a chemical compound resulting from the combination of 1,2-dihydroacenaphthylene and 1,3,5-trinitrobenzene in a 1:1 ratio. 1,2-Dihydroacenaphthylene is a polycyclic aromatic hydrocarbon with a molecular formula of C12H10, characterized by its two fused benzene rings and a saturated six-membered ring. 1,3,5-Trinitrobenzene, on the other hand, is a nitroaromatic compound with a molecular formula of C6H3N3O6, featuring three nitro groups attached to a benzene ring. The 1:1 mixture of these two chemicals results in a complex molecule with potential applications in various fields, such as materials science and organic synthesis. However, due to the presence of nitro groups in 1,3,5-trinitrobenzene, 1,2-dihydroacenaphthylene - 1,3,5-trinitrobenzene (1:1) may exhibit explosive properties, and thus, proper safety precautions should be taken when handling and storing it.

5892-43-3

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5892-43-3 Usage

Components

The compound consists of two main components 1,2-dihydroacenaphthylene, a polycyclic aromatic hydrocarbon, and 1,3,5-trinitrobenzene, a highly explosive compound.

Structure

The structure of the compound is likely to be complex due to the combination of two different types of molecules.

Explosive properties

Given the explosive nature of 1,3,5-trinitrobenzene, the resulting compound is likely to have explosive properties.

Potential applications

The compound may have potential applications in military and industrial settings due to its explosive properties, although exact details are not widely available.

Stability

The stability of the compound is not known, but it may be influenced by the stability of its constituent components.

Reactivity

The reactivity of the compound is not known, but it may be influenced by the reactivity of its constituent components.

Physical properties

The physical properties of the compound, such as its appearance, density, and melting/boiling points, are not known.

Chemical properties

The chemical properties of the compound, such as its reactivity with other substances and its chemical stability, are not known.

Safety

The safety of the compound is not known, but given the explosive nature of 1,3,5-trinitrobenzene, it is likely to be a hazardous material that requires careful handling and storage.

Check Digit Verification of cas no

The CAS Registry Mumber 5892-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,9 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5892-43:
(6*5)+(5*8)+(4*9)+(3*2)+(2*4)+(1*3)=123
123 % 10 = 3
So 5892-43-3 is a valid CAS Registry Number.

5892-43-3SDS

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 1,2-dihydroacenaphthylene,1,3,5-trinitrobenzene

1.2 Other means of identification

Product number -
Other names acenaphthene,compound with 1,3,5-trinitro-benzene

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:5892-43-3 SDS

5892-43-3Downstream Products

5892-43-3Relevant academic research and scientific papers

Molecular complexes of 1,3,5-trinitrobenzene with naphthalene and its derivatives

Pryalkin

experimental part, p. 2359 - 2366 (2010/05/02)

The relation between spectral parameters of molecular complexes formed by 1,3,5-trinitrobenzene with naphthalene derivatives and ionization potentials of the donor molecule is discussed. The molecular complexes were divided into three groups: naphthalene, naphthalene-1-amine, and naphthalene-2-amine derivatives. This division was substantiated in terms of the existence of several intermolecular interactions between the components and steric structure of the complexes. Problems related to classification of molecular complexes are discussed.

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