Skip to main content

2,6-Dichloro-4-nitroaniline

ADVERTISEMENT
Identification
Molecular formula
C6H4Cl2N2O2
CAS number
99-30-9
IUPAC name
2,6-dichloro-4-nitro-aniline
State
State
2,6-Dichloro-4-nitroaniline is a solid at room temperature.
Melting point (Celsius)
214.00
Melting point (Kelvin)
487.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
207.02g/mol
Molar mass
207.0150g/mol
Density
1.6960g/cm3
Appearence

2,6-Dichloro-4-nitroaniline is a solid compound that appears as a yellow crystalline powder.

Comment on solubility

Solubility of 2,6-Dichloro-4-nitro-aniline

2,6-Dichloro-4-nitro-aniline, a compound known for its aromatic structure, displays particular solubility characteristics that are important for its applications and interactions in various environments. The solubility of this compound can be influenced by several factors, including:

  • Polarity: The presence of the nitro group (–NO2) contributes to a polar character, which can enhance solubility in polar solvents.
  • Chlorine Substitution: The chlorinated positions on the aniline ring may hinder solubility in non-polar solvents, leading to preferential solubility in organic solvents like ethyl acetate and dimethyl sulfoxide (DMSO).
  • Hydrogen Bonding: The amino group (-NH2) has the potential to form hydrogen bonds, increasing solubility in water to some extent, although steric hindrance by the chlorines may limit this effect.

It is important to note that while this compound has moderate solubility in common solvents, its solubility may not be ideal for all applications. Typical solubility observations include:

  1. Moderate solubility in water, potentially leading to limited applications in aqueous environments.
  2. Better solubility profiles in organic solvents, enhancing its applicability in organic synthesis and chemical reactions.

In summary, 2,6-dichloro-4-nitro-aniline demonstrates a blend of solubility traits influenced by its molecular structure. Understanding these solubility aspects is crucial for optimizing its use in chemistry and related fields.

Interesting facts

Interesting Facts About 2,6-Dichloro-4-Nitro-Aniline

2,6-Dichloro-4-nitro-aniline is a fascinating compound that is known for its unique chemical structure and versatile applications. As a member of the aniline family, it combines several functional groups that impart distinct characteristics.

Key Characteristics:

  • Dichloro substituents: The presence of chlorine atoms in the 2 and 6 positions of the aromatic ring enhances the compound's reactivity and stability.
  • Nitro group: The electron-withdrawing nitro group at the 4-position contributes to the compound’s functionality in various chemical reactions, making it an important intermediate in organic synthesis.
  • Amine functionality: As an aniline derivative, it possesses an amino (-NH2) group, allowing it to participate in a variety of chemical processes including coupling reactions.

Applications:

This compound has several noteworthy applications in different fields:

  • Dyes and Pigments: Its vibrant color properties make it a candidate for use in the synthesis of dyes and pigments.
  • Pesticides: The compound is utilized in the development of certain agrochemicals, demonstrating its utility in protecting crops.
  • Pharmaceuticals: As a synthetic intermediate, it may play a role in the development of pharmaceutical agents, showcasing its versatility in medicinal chemistry.

Safety and Handling:

Handling 2,6-Dichloro-4-nitro-aniline requires caution due to its potential toxicity. Proper personal protective equipment (PPE) should always be used, and safety protocols followed, as with any chemical compound.

A Final Note:

In the world of chemistry, compounds like 2,6-Dichloro-4-nitro-aniline illustrate the complexity and diversity of chemical structures. As chemists explore and utilize such compounds, the potential for discovery remains vast. As they say in chemistry, “The properties of a compound are often defined by its structure.” Happy experimenting!

Synonyms
2,6-DICHLORO-4-NITROANILINE
99-30-9
Dichloran
Dicloran
Allisan
Botran
DCNA
Ditranil
Bortran
Resisan
2,6-Dichloro-4-nitrobenzenamine
Benzenamine, 2,6-dichloro-4-nitro-
Batran
2,6-Dichlor-4-nitroanilin
DCNA (fungicide)
CDNA
4-Nitro-2,6-dichloroaniline
Dicloran [BSI]
Botran 45W
Dichloran (amine fungicide)
AL-50
Aniline, 2,6-dichloro-4-nitro-
CCRIS 3111
RD-6584
4-Nitroaniline, 2,6-dichloro-
HSDB 1570
NSC 218
UNII-F0BE9UC5J7
EINECS 202-746-4
Botran 75b
Botran 75w
U-2069
EPA Pesticide Chemical Code 031301
BRN 1459581
CURITAL
FUBOTRAN
GRIMACIT
REGESAN
RESINAN
2,6-dichloro-4-nitro-aniline
CNA
DTXSID2020426
CHEBI:27864
AI3-08870
NSC-218
DICLORAN [HSDB]
MFCD00007677
F0BE9UC5J7
2,6-Dichloro-p-nitroaniline
DTXCID60426
2,6-Dichloro-4-nitrobenzeneamine
4-12-00-01681 (Beilstein Handbook Reference)
1-Amino-2,6-dichloro-4-nitrobenzene
Caswell No. 311
alizan
CAS-99-30-9
2,?6-?Dichloro-?4-?nitroaniline (Dichloran)
AI3-08870 (USDA)
2,6-Dichlor-4-nitroanilin [Czech]
2,6-dichlor-4-nitroaniline
2,6-Dichloro-4-nitroaniline-13C6(Dichloran-13C6)
DCNA(FUNGICIDE)
2,6Dichlor4nitroanilin
2,6Dichloro4nitroaniline
4Nitro2,6dichloroaniline
2,6-dichloro-4nitroaniline
WLN: ZR BG FG DNW
4-Nitroaniline,6-dichloro-
4Nitroaniline, 2,6dichloro
2,6-dichloro-4-nitroanilin
2,6Dichloro4nitrobenzenamine
MLS002152899
Aniline,6-dichloro-4-nitro-
BIDD:ER0704
Dichloran, analytical standard
SCHEMBL229362
CHEMBL504381
NSC218
Benzenamine,6-dichloro-4-nitro-
DICHLORAN(AMINE FUNGICIDE)
STR00347
Tox21_202341
Tox21_300838
RD6584
STK391975
2,6-Dichloro-4-nitroaniline, 96%
Dicloran 10 microg/mL in Cyclohexane
AKOS000120531
AKOS040744733
CS-W021045
FD14274
2, 6 - dichloro - 4 - nitroaniline
NCGC00091358-01
NCGC00091358-02
NCGC00091358-03
NCGC00091358-04
NCGC00091358-05
NCGC00254742-01
NCGC00259890-01
AC-11325
SMR000777926
DB-057776
D0385
NS00006107
U2069
Dichloran, PESTANAL(R), analytical standard
EN300-20800
D78131
Q2217808
Dichloran, certified reference material, TraceCERT(R)