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DNOC (4,6-Dinitro-o-cresol)

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Identification
Molecular formula
C7H3Cl3NO
CAS number
133-59-1
IUPAC name
2,6-dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one
State
State

At room temperature, 2,6-Dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one is typically found in a solid state. It is known to have a crystalline form which is characteristic for many aromatic compounds, allowing easy handling and application in various chemical processes.

Melting point (Celsius)
87.20
Melting point (Kelvin)
360.35
Boiling point (Celsius)
322.00
Boiling point (Kelvin)
595.15
General information
Molecular weight
263.46g/mol
Molar mass
263.0000g/mol
Density
1.6830g/cm3
Appearence

2,6-Dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one, also known as "DNOC," typically appears as a solid of yellow to orange crystals. It is often encountered in its crystalline form and is known for its intense coloration which results from the chromophoric nature of the nitro groups present in its structure.

Comment on solubility

Solubility of 2,6-Dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one

The solubility of 2,6-dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one in various solvents can provide insight into its behavior in different chemical environments. This compound exhibits unique structural characteristics that influence its solubility profile:

  • Polarity: The presence of chlorine substituents on the cyclohexadiene ring can enhance the compound's polarity, which may improve its solubility in polar solvents such as water and alcohols.
  • Non-polar Solvents: Conversely, due to its rigid cyclic structure, 2,6-dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one is likely to have limited solubility in non-polar solvents like hexane or benzene.
  • Solvent Interactions: The interactions with solvents can be further explored through solubility testing in a range of liquid media, potentially revealing optimal conditions for its use in reactions or formulations.

Experimentation will reveal the precise solubility characteristics; however, considering its chemical structure and functional groups, researchers may anticipate moderate to high solubility in polar environments, thus enhancing its applicability in various fields of chemistry.

Interesting facts

Exploring 2,6-Dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one

2,6-Dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one is a fascinating compound that lies at the intersection of synthesis and application in organic chemistry. This compound is known for its unique structure and properties, making it a subject of interest in various chemical fields.

Key Features:

  • Chloro Groups: The presence of multiple chlorine substituents within the molecular framework enhances its reactivity and stability, allowing for interesting chemical transformations.
  • Imine Group: The imino (-C=NH) functional group plays a crucial role in the compound's reactivity, promoting potential pathways for synthesis and applications in materials science.
  • Cyclohexadiene Framework: The cyclic structure contributes to the compound's unique electronic properties, potentially influencing how it interacts with other chemical entities.

This compound can serve as a versatile intermediate in synthetic organic chemistry. Researchers have explored pathways for utilizing its derived functional properties in:

  • Organic synthesis, contributing to the development of novel compounds.
  • Potential biomedical applications, in which its unique structure may play a role in targeting specific biological pathways.
  • Light-sensitive materials that leverage the compound's specific electronic characteristics.

As with many compounds, understanding the properties of 2,6-dichloro-4-chloroimino-cyclohexa-2,5-dien-1-one can require a multidisciplinary approach combining organic chemistry, materials science, and pharmacology.

In the words of a prominent chemist, "Innovation in chemistry lies within the nuances of molecular interactions and transformations." This compound exemplifies such innovation, offering a myriad of possibilities for future research and development.

Synonyms
2,6-Dichloroquinone-4-chloroimide
101-38-2
Gibbs reagent
2,6-Dichloro-4-(chloroimino)cyclohexa-2,5-dienone
2,5-Cyclohexadien-1-one, 2,6-dichloro-4-(chloroimino)-
2,6-Dichloroquinone chloroimide
2,6-Dichloroquinonechloroimine
N,2,6-Trichlorobenzoquinone imine
2,6-Dichloroquinone-4-chloroimine
2,6-Dichlorobenzoquinone chloroimide
2,6-Dichloro-4-N-chloroquinonimine
p-Benzoquinone imine, N,2,6-trichloro-
n,2,6-trichloroquinoneimine
NSC 6293
N,2,6-Trichloro-p-benzoquinonimine
AI3-52333
N,2,6-Trichloro-p-benzoquinone imine
C6H2Cl3NO
EINECS 202-937-2
N,2,6-Trichloro-4-benzoquinone imine
BRN 2364249
Y19A13RZO0
N,2,6-Trichloro-p-quinoneimine
4-Chloroimino-2,6-dichloro-2,5-cyclohexadiene-1-one
2,6-Dichloro-4-(chloroimino)-2,5-cyclohexadien-1-one
NSC-6293
MFCD00001611
2,5-CYCLOHEXADIEN-1-ONE, 4-CHLOROIMINO-2,6-DICHLORO-
GIBBS REAGENT [MI]
DTXSID2059229
3-07-00-03377 (Beilstein Handbook Reference)
N-2,6-Trichloro-p-benzoquinonimine
2,6-dichloro-4-(chloroimino)cyclohexa-2,5-dien-1-one
N,2,6-Trichloro-p-benzoquinone Monoimine
2,6-Dichloroquinone-4-chloroimide (>90%)
UNII-Y19A13RZO0
Gibb's reagent
Gibbs' reagent
2,6-dichloro-4-chloroiminocyclohexa-2,5-dien-1-one
dichloroquinonechlorimide
2,6-Dichloro-1,4-quinone-4-chlorimide
2,6Dichloroquinonechloroimine
SCHEMBL478999
2,6Dichloroquinone chloroimide
2,6Dichloroquinone4chloroimide
2,6Dichloroquinone4chloroimine
2,6Dichloro4Nchloroquinonimine
N,2,6Trichloropbenzoquinonimine
N,6-Trichlorobenzoquinone imine
CHEMBL3276931
DTXCID0032578
YHUMTHWQGWPJOQ-UHFFFAOYSA-
N,2,6Trichlorobenzoquinone imine
N,6-Trichloro-p-benzoquinonimine
NSC6293
2,6-Dichloroquinone-4-chlorimide
N,2,6Trichloropbenzoquinone imine
WLN: L6V DYJ BG DUNG FG
2, 4-chloroimino-2,6-dichloro-
2,6Dichlorobenzoquinone chloroimide
N,2,6-trichloro-4-benzoquinoneimine
N,2,6-Trichloro-p-benzoquinoneimide
p-Benzoquinone imine,2,6-trichloro-
pBenzoquinone imine, N,2,6trichloro
2, 2,6-dichloro-4-(chloroimino)-
AKOS015901257
N-2,6-Trichloro-p-benzoquinone imine
FS-4501
HY-W105135
2,6-Dichloro-p-benzoquinone-4-chlorimine
PD197261
SY048612
2,6-Dichloroquinone-4-chloroimide, 99.0%
4Chloroimino2,6dichloro2,5cyclohexadiene1one
CS-0157777
NS00023054
T0397
2,6Dichloro4(chloroimino)cyclohexa2,5dienone
2,5Cyclohexadien1one, 4chloroimino2,6dichloro
2,6Dichloro4(chloroimino)2,5cyclohexadien1one
D88188
2,5Cyclohexadien1one, 2,6dichloro4(chloroimino)
Q209277
2,6-Dichloro-4-(chloroimino)-2,5-cyclohexadien-1-one #
InChI=1/C6H2Cl3NO/c7-4-1-3(10-9)2-5(8)6(4)11/h1-2H
2,6-Dichloroquinone-4-chloroimide, for spectrophotometric det. of vitamin B6, >=99.0%