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Identification
Molecular formula
C12H17N + C16H16O2
CAS number
.
IUPAC name
4-phenylcyclohexanamine;2-(4-phenylphenyl)butanoic acid
State
State
The state of this compound at room temperature can vary depending on its mixed composition and preparation method.
Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
372.52g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence
The appearance of this compound is not documented. It is a multi-component system that may have a different appearance than its individual components.
Comment on solubility

Solubility of 4-phenylcyclohexanamine and 2-(4-phenylphenyl)butanoic acid

The solubility of a compound can provide insight into its chemical behavior and potential applications. In the case of 4-phenylcyclohexanamine and 2-(4-phenylphenyl)butanoic acid, we observe distinct characteristics based on their structural features.

4-Phenylcyclohexanamine

  • Solvent Interactions: Generally soluble in organic solvents such as ethanol and chloroform, due to its aromatic ring and amine functional group.
  • Water Solubility: Limited water solubility due to the hydrophobic cyclohexane structure and the bulky phenyl group.

2-(4-phenylphenyl)butanoic acid

  • Solubility in Organic Solvents: It is likely soluble in organic solvents because of the presence of multiple phenyl groups which enhance van der Waals interactions with non-polar solvents.
  • Hydrophilicity: The presence of the carboxylic acid group can contribute to some degree of solubility in polar solvents, although overall solubility may still be moderate due to steric hindrance from the aromatic rings.

In summary, while both compounds exhibit varied solubility profiles, their structural components significantly influence their interactions with different solvents. Understanding these solubility characteristics is essential for predicting their behavior in chemical reactions and biological systems.

Interesting facts

Interesting Facts about 4-Phenylcyclohexanamine and 2-(4-phenylphenyl)butanoic Acid

The compound 4-phenylcyclohexanamine and its counterpart 2-(4-phenylphenyl)butanoic acid represent intriguing examples within the realm of organic chemistry, showcasing the versatility and complexity of amines and carboxylic acids.

Unique Properties and Applications

These compounds are notable not only for their chemical structures but also for their potential applications in various fields:

  • Pharmaceutical Research: Both compounds have been explored in medicinal chemistry, contributing to drug design and development.
  • Material Science: Their unique structural characteristics make them candidates for use in polymers and advanced materials.
  • Biological Studies: Due to the phenyl groups in their structures, these compounds can interact with biological systems, which is essential for understanding drug interactions.

Why They Matter

The structural elements of these compounds provide a canvas for diverse chemical reactivity. For example:

  • 4-phenylcyclohexanamine features a cyclohexane ring, and modifying this ring can lead to interesting chemical behaviors.
  • 2-(4-phenylphenyl)butanoic acid showcases how functionalities can impact solubility and interaction with various receptor sites in biological molecules.

As chemists, we often quote, "The structure determines the function." This saying rings especially true for these compounds, where their spatial configuration plays a crucial role in their chemical properties and biological activity.

Research Opportunities

For aspiring chemistry students, studying these compounds opens a door to numerous research opportunities, including:

  • Exploring synthesis methods to create new derivatives.
  • Investigating their potential roles in treating neurological disorders.
  • Analyzing their stability and reactivity under various conditions.

In conclusion, both 4-phenylcyclohexanamine and 2-(4-phenylphenyl)butanoic acid exemplify the depth and complexity of organic compounds, encouraging further exploration in both theoretical and applied chemistry.

Synonyms
Butixirate
19992-80-4
Flectar
MG5771;Flectar
M.G. 5771
cis-M.G. 5771
4-phenylcyclohexan-1-amine;2-(4-phenylphenyl)butanoic acid
NIOSH/DU8331700
82CYO8A460
DU83317000
Butixirato
Butixiratum
Butixirate [USAN:INN]
Butixiratum [INN-Latin]
Butixirato [INN-Spanish]
EINECS 243-454-7
MG 5771
UNII-82CYO8A460
trans-4-Phenylcyclohexylamin 2-(4-biphenylyl)butyrat
Xenbucin trans-4-phenylcyclohexylamine salt
BUTIXIRATE [INN]
Butixirate (USAN/INN)
BUTIXIRATE [USAN]
BUTIXIRATE [MART.]
(+-)-alpha-Ethyl-4-biphenylacetic acid, compound with trans-4-phenylcyclohexylamine (1:1)
SCHEMBL120698
orb1698000
SCHEMBL29508495
DTXSID60941965
KWFFVBCJCQQAIV-UHFFFAOYSA-N
XENBUCIN PHENYLCYCLOHEXYLAMINE
AKOS040750942
MG-5771
(1,1'-Biphenyl)-4-acetic acid, alpha-ethyl-, (+-)-, compound with trans-4-phenylcyclohexanamine (1:1)
NS00083263
D03193
Q27269320
XENBUCIN TRANS-4-PHENYLCYCLOHEXYLAMINE SALT (1:1)
XENBUCIN TRANS-4-PHENYLCYCLOHEXYLAMINE SALT (1:1) [MI]
2-([1,1'-Biphenyl]-4-yl)butanoic acid--4-phenylcyclohexan-1-amine (1/1)
(+/-)-.ALPHA.-ETHYL-4-BIPHENYLACETIC ACID, COMPOUND WITH TRANS-4-PHENYLCYCLOHEXYLAMINE (1:1)
(1,1'-BIPHENYL)-4-ACETIC ACID, .ALPHA.-ETHYL-, (+/-)-, COMPOUND WITH TRANS-4-PHENYLCYCLOHEXANAMINE (1:1)