Interesting facts
Interesting Facts about 1,3-Dinitronaphthalene
1,3-Dinitronaphthalene, often abbreviated as 1,3-DN, is a fascinating chemical compound that belongs to the class of nitronaphthalenes. Here are some intriguing aspects that showcase its significance and multifaceted nature:
- Structure and Isomerism: The compound is known for its dynamic structure characterized by two nitro groups attached to different positions on the naphthalene ring. This leads to a vivid example of positional isomerism, where the nitro groups can be oriented differently, impacting the compound's reactivity and properties.
- Historical Importance: 1,3-Dinitronaphthalene has played a critical role in organic chemistry and industrial applications, particularly as a precursor in the synthesis of dyes, explosives, and other important chemical intermediates.
- Applications in Research: This compound is frequently utilized in scientific research, especially in the study of electron-deficient systems. Researchers often investigate its behavior in electrophilic aromatic substitution reactions, assisting in understanding fundamental concepts in both organic and physical chemistry.
- Toxicity Considerations: It’s important to handle 1,3-Dinitronaphthalene with care due to its potential health hazards. As a member of nitroaromatic compounds, it is considered hazardous and poses environmental concerns; thus, appropriate safety protocols must be adhered to in any lab setting.
- Analytical Techniques: This compound showcases fascinating properties that make it amenable to a variety of analytical techniques, such as gas chromatography and mass spectrometry. These techniques allow chemists to examine its presence and concentration in various samples.
In conclusion, 1,3-Dinitronaphthalene stands out as more than just a simple chemical compound. Its significance spans multiple fields, including industrial chemistry, environmental science, and academic research. Understanding its properties opens up avenues for innovation and exploration in chemistry.
Synonyms
1,3-DINITRONAPHTHALENE
606-37-1
Naphthalene, 1,3-dinitro-
CCRIS 6027
EINECS 210-116-5
UNII-D55U333CQS
NSC 74478
BRN 1976375
D55U333CQS
DTXSID9025164
CHEBI:50638
AI3-26488
NSC-74478
DTXCID105164
ULALSFRIGPMWRS-UHFFFAOYSA-
DINITRONAPHTHALENE, 1,3-
4-05-00-01680 (Beilstein Handbook Reference)
210-116-5
inchi=1/c10h6n2o4/c13-11(14)8-5-7-3-1-2-4-9(7)10(6-8)12(15)16/h1-6h
ulalsfrigpmwrs-uhfffaoysa-n
1,3-dinitro-naphthalene
NCGC00091210-02
Naphthalene,3-dinitro-
SCHEMBL57381
1,3-Dinitronaphthalene 10 microg/mL in Cyclohexane
1,3-Dinitronaphthalene, 97%
CHEMBL163970
NSC74478
Tox21_400056
MFCD00003915
AKOS016009682
FD33581
NCGC00091210-01
NCGC00091210-03
AS-18939
CAS-606-37-1
DB-053676
CS-0363755
NS00034411
A10830
Q27122160
Solubility of 1,3-Dinitronaphthalene
1,3-Dinitronaphthalene, with the chemical formula C10H6N2O4, demonstrates some intriguing properties when it comes to solubility. Its ability to dissolve in various solvents can be characterized as follows:
To sum up, 1,3-dinitronaphthalene is insoluble in water but soluble in a variety of organic solvents. This information is vital for its use in chemical applications, where appropriate solvent selection is crucial for desired reactions and processes.