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Loronoxinol

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Identification
Molecular formula
C12H17N3O4
CAS number
131-89-5
IUPAC name
N-cyclohexylcyclohexanamine;2-cyclohexyl-4,6-dinitro-phenol
State
State

At room temperature, Loronoxinol is in a solid state. It is a stable compound under normal conditions, but sensitivity to heat and light should be considered due to the presence of nitro groups.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.00
Boiling point (Celsius)
181.00
Boiling point (Kelvin)
454.00
General information
Molecular weight
292.33g/mol
Molar mass
292.3290g/mol
Density
1.2650g/cm3
Appearence

Loronoxinol appears as a yellow crystalline solid. The compound's vivid color is due to its dinitrophenol component, which is characteristic of many nitroaromatic compounds that tend to absorb light in the visible range.

Comment on solubility

Solubility of N-cyclohexylcyclohexanamine; 2-cyclohexyl-4,6-dinitro-phenol

The solubility profile of N-cyclohexylcyclohexanamine and 2-cyclohexyl-4,6-dinitro-phenol offers interesting insights into their chemical behavior and potential applications.

N-cyclohexylcyclohexanamine

  • This compound typically exhibits limited solubility in water because of its bulkiness and hydrophobic cyclohexyl groups.
  • However, it may dissolve well in organic solvents such as ethanol, acetone, and chloroform due to favorable interactions with nonpolar solvents.

2-cyclohexyl-4,6-dinitro-phenol

  • 2-cyclohexyl-4,6-dinitro-phenol is generally expected to be poorly soluble in water, primarily due to the presence of the large cyclohexyl group and multiple nitro substituents that increase steric hindrance.
  • It is likely to show reasonable solubility in organic solvents, particularly those that are less polar.

In summary, both compounds demonstrate varying solubility characteristics strongly influenced by their molecular structure. Compounds with large nonpolar groups tend to be soluble in organic mediums while showing limited solubility in aqueous environments. Understanding these solubility traits is crucial for practical applications, whether it be in synthesis, formulation, or environmental considerations.

Interesting facts

N-cyclohexylcyclohexanamine

N-cyclohexylcyclohexanamine is an intriguing compound that showcases the fascinating world of amines. As a member of the cyclohexyl amines family, it exhibits a unique structure that can lead to interesting chemical behaviors and applications. Here are some key points to consider:

  • Structure: The compound features two cyclohexyl groups, which impact its steric and electronic properties significantly.
  • Applications: It has been researched for its potential uses in pharmaceuticals and agrochemicals, where the amine functional group plays a crucial role in reactivity.
  • Synthesis: Chemists can synthesize N-cyclohexylcyclohexanamine through various methods, often employing reactions that modify existing amines or generate new cyclic structures.
  • Reactivity: The amine group can engage in hydrogen bonding, influencing solubility and interactions with other compounds in chemical reactions.

As a scientist or student in the field of chemistry, studying such compounds offers insight into their potential functional uses and the underlying principles of molecular structures.

2-cyclohexyl-4,6-dinitro-phenol

2-cyclohexyl-4,6-dinitro-phenol, also known colloquially as a nitrated phenolic compound, is another notable chemical in the realm of organic synthesis. Its structure, characterized by cyclohexyl and nitro substituents on a phenolic ring, provides a wealth of interesting features:

  • Nitro Groups: The presence of two nitro groups significantly influences the compound’s reactivity, making it a potential candidate for various chemical transformations.
  • Biological Impact: Such compounds are often evaluated for their biological activity, which may include antimicrobial properties or effects on plants, making them of interest in both medicinal and agricultural chemistry.
  • Stability and Safety: Understanding the environmental stability and safety of dinitrophenols is crucial, as they can pose hazards if not managed properly in laboratory settings.
  • Applications in Research: Compounds like 2-cyclohexyl-4,6-dinitro-phenol are frequently used as intermediates in the synthesis of more complex chemicals or as reagents in organic reactions.

As students or researchers explore this compound, they not only learn about its chemical properties but also the broader implications and responsibilities associated with working with nitro compounds.

Synonyms
Dinex-diclexine
Dynone II
Dn Cust D-4
Dinex-diclexine [ISO]
Caswell No. 330
317-83-9
Dicyclohexylamine salt of dinex
Dicyclohexylamine, salt of dnochp
DN 111
DN-111
ENT 30,838
Dicyclohexylamine 4,6-dinitro-o-cyclohexylphenate
Dicyclohexylammonium 2-cyclohexyl-4,6-dinitrophenate
NSC 5749
2-Cyclohexyl-4,6-dinitrophenol dicyclohexylamine salt
UNII-D1401W3XFU
Dinitrocyclohexylphenol, dicyclohexylamine salt
D1401W3XFU
Dicyclohexylammonium 4,6-dinitro-o-cyclohexylphenate
Dicyclohexylamine salt of 4,6-dinitro-o-cyclohexylphenol
NSC-5749
2-Cyclohexyl-4,6-dinitrophenol dicyclohexylamine
Dicyclohexylamine 4,6-dinitro-o-cyclohexylphenolate
Dinitro-o-cyclohexylphenol (dicyclohexylamine salt)
2-Cyclohexyl-4,6-dinitrophenol, dicyclohexylamine salt
4,6-Dinitro-o-cyclohexylphenol, dicyclohexylamine salt
DTXSID8074990
4, dicyclohexylamine salt
DTXCID6038405
SCHEMBL11718645
2-CYCLOHEXYL-4,6-DINITROPHENOL DICYCLO HEXYLAMINE
NSC5749
2-Cyclohexyl-4, dicyclohexylamine
2-Cyclohexyl-4, dicyclohexylamine salt
Dicyclohexylamine,6-dinitrophenol (1:1)
Ammonium, 2-cyclohexyl-4,6-dinitrophenate
DS-004046
WLN: L6TJ AR BQ CNW ENW & 621
Phenol,6-dinitro-, compd with dicylohexylamine
Dinitro-o-cyclohexylphenol, dicyclohexylamine salt
Q27275958
Phenol, 2-cyclohexyl-4,6-dinitro-, compd. with dicyclohexylamine (1:1) (8CI)
Phenol, 2-cyclohexyl-4,6-dinitro-, compd. with N-cyclohexylcyclohexanamine (1:1) (9CI)