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2-Bromo-4,6-dinitroaniline

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Identification
Molecular formula
C6H4BrN3O4
CAS number
1817-73-8
IUPAC name
2-bromo-4,6-dinitro-aniline
State
State

At room temperature, 2-Bromo-4,6-dinitroaniline is a solid. It typically presents itself in a crystalline form and maintains stability under normal conditions.

Melting point (Celsius)
124.00
Melting point (Kelvin)
397.15
Boiling point (Celsius)
335.00
Boiling point (Kelvin)
608.15
General information
Molecular weight
262.02g/mol
Molar mass
263.0310g/mol
Density
2.0770g/cm3
Appearence

2-Bromo-4,6-dinitroaniline is a yellow crystalline solid. The crystals may appear in the form of either powder or small granules, and it is typically characterized by its bright yellow coloration.

Comment on solubility

Solubility of 2-bromo-4,6-dinitro-aniline

The solubility of 2-bromo-4,6-dinitro-aniline in various solvents can be intriguing due to its functional groups and molecular structure. This compound is known to exhibit different solubility behaviors based on the solvent selected, influenced by its polar and non-polar characteristics. Below are some notable points regarding its solubility:

  • Water: 2-bromo-4,6-dinitro-aniline is generally considered to be insoluble in water due to the hydrophobic nature of the bromine and dinitro groups.
  • Organic Solvents: It shows better solubility in organic solvents such as ethanol, acetone, and dichloromethane due to the ability of these solvents to interact with aromatic compounds.
  • Acidity and Basicity: The presence of amino groups can affect solubility. In more acidic conditions, protonation may help improve solubility in polar solvents.

In summary, the solubility of 2-bromo-4,6-dinitro-aniline can be summarized as:

  1. Insoluble in water.
  2. Soluble in polar organic solvents.
  3. Potential increase in solubility through protonation in acidic environments.

Understanding the solubility of such compounds is crucial for applications in areas like pharmaceuticals and chemical synthesis, where solvent choice can greatly influence the reaction outcomes.

Interesting facts

Interesting Facts about 2-bromo-4,6-dinitro-aniline

2-bromo-4,6-dinitro-aniline is an intriguing aromatic compound that has generated considerable interest in the field of chemistry. This compound offers a wealth of fascinating properties and applications, making it a subject of study for both students and professionals alike. Here are some interesting highlights:

  • Chemical Structure: As an aniline derivative, this compound features an amine group attached to a benzene ring, which is substituted at specific positions. The presence of nitro groups and a bromo atom greatly influences its reactivity and physical properties.
  • Industrial Applications: 2-bromo-4,6-dinitro-aniline is valued in the synthesis of dyes and pigments due to its vibrant color characteristics. It is often utilized in the production of azo dyes, which are prominent in the textile industry.
  • Research Relevance: This compound serves as a key intermediate in various chemical reactions, making it valuable in organic synthesis. Its reactivity allows chemists to explore diverse pathways for creating new materials and compounds.
  • Biological Activity: Some studies have suggested that derivatives of 2-bromo-4,6-dinitro-aniline exhibit antifungal and antibacterial properties. This opens up potential avenues for pharmaceutical research and development.
  • Environmental Considerations: Given its nitro groups, there are concerns regarding the environmental impact and toxicity of 2-bromo-4,6-dinitro-aniline. Studies focus on its degradation and the implications of its use in consumer products.

In summary, 2-bromo-4,6-dinitro-aniline is not just a simple chemical compound; it embodies the intersection of industrial application, research significance, and environmental awareness. As emphasized by chemists, "*Understanding the multifaceted properties of such compounds is crucial for advancing material science and catering to sustainable practices.*" It remains a topic of ongoing research and discussion in the chemical community.

Synonyms
2-BROMO-4,6-DINITROANILINE
1817-73-8
Benzenamine, 2-bromo-4,6-dinitro-
6-Bromo-2,4-dinitroaniline
2,4-Dinitro-6-bromoaniline
Bromo DNA
2-Bromo-4,6-dinitroaminobenzene
Aniline, 2-bromo-4,6-dinitro-
2,4-Dinitro-6-bromanilin
NCI-C60844
Aniline, 2,4-dinitro-6-bromo-
CCRIS 820
NSC 16572
HSDB 5453
2,4-Dinitro-6-bromanilin (czech)
EINECS 217-329-2
2,4-Dinitro-6-bromoanilin
2,4-Dinitro-6-bromoanilin [Czech]
Benzenamide, 2-bromo-4,6-dinitro-
BRN 0916722
2-bromo-4,6-dinitrobenzenamine
DTXSID4024646
NSC-16572
DTXCID204646
105X73C593
4-12-00-01734 (Beilstein Handbook Reference)
2,4-Dinitro-6-bromanilin [Czech]
2-BROMO-4,6-DINITROANILINE [HSDB]
2,4-DINITRO-6-BROMOANILIN (CZECH)
2,4Dinitro6bromanilin
2,4Dinitro6bromoanilin
2,4Dinitro6bromoaniline
6Bromo2,4dinitroaniline
Aniline, 2,4dinitro6bromo
Aniline, 2bromo4,6dinitro
2Bromo4,6dinitroaminobenzene
Benzenamide, 2bromo4,6dinitro
217-329-2
MFCD00007146
MLS002152870
2-bromanyl-4,6-dinitro-aniline
2-Bromo-4,6-dinitro-benzenamine
SMR001224488
UNII-105X73C593
2,4-Dinitro-6-bromanilin [Czech]
2,4-Dinitro-6-bromaniline
WLN: WNR BZ CE ENW
Aniline,4-dinitro-6-bromo-
cid_15752
SCHEMBL909587
2,4-dinitro-6-bromo-aniline
CHEMBL167513
BDBM74244
HMS3039A09
NSC16572
(2-bromo-4,6-dinitro-phenyl)amine
aniline, 2-bromo-4,6-dinitro- -
Tox21_200070
2-Bromo-4,6-dinitroaniline, 94%
AKOS015912484
AKOS015967540
NCGC00091598-01
NCGC00091598-02
NCGC00257624-01
AC-11795
AS-61318
SY057093
CAS-1817-73-8
DB-044442
B0814
CS-0157748
NS00006845
H11796
A812636
SR-01000312697
SR-01000312697-1
Q27251119
InChI=1/C6H4BrN3O4/c7-4-1-3(9(11)12)2-5(6(4)8)10(13)14/h1-2H,8H