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1-Aminocyclohexane-1,3-dicarboxylic acid

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Identification
Molecular formula
C8H13NO4
CAS number
49710-13-2
IUPAC name
1-aminocyclohexane-1,3-dicarboxylic acid
State
State
At room temperature, this compound is usually in a solid state. Its crystalline structure and white to off-white coloration are typical characteristics.
Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
285.00
Boiling point (Kelvin)
558.15
General information
Molecular weight
173.19g/mol
Molar mass
173.1880g/mol
Density
1.4500g/cm3
Appearence

1-Aminocyclohexane-1,3-dicarboxylic acid typically appears as a white to off-white crystalline powder. The compound is usually found in solid form at room temperature.

Comment on solubility

Solubility of 1-Aminocyclohexane-1,3-dicarboxylic Acid

1-Aminocyclohexane-1,3-dicarboxylic acid, with the chemical formula C8H13NO4, exhibits interesting solubility characteristics due to its unique structure and functional groups. The presence of both amino and carboxylic acid groups contributes to its solubility profile:

  • Solvent Interaction: This compound is likely to be soluble in polar solvents such as water. The carboxylic acid groups can form hydrogen bonds with water molecules, effectively enhancing solubility.
  • Solubility in Organic Solvents: While it is expected to be predominantly soluble in polar solvents, its solubility in non-polar organic solvents may be limited due to the increased hydrophobic nature of the cyclohexane ring.
  • Temperature Influence: Like many other organic acids, the solubility of 1-aminocyclohexane-1,3-dicarboxylic acid may increase with temperature, reflecting the general trend in solubility behavior.

Due to these factors, it is essential to consider the solvent environment when assessing the solubility of this compound. In practical applications, choosing the right solvent can significantly affect the behavior and reactivity of 1-aminocyclohexane-1,3-dicarboxylic acid.

Interesting facts

Interesting Facts about 1-Aminocyclohexane-1,3-dicarboxylic Acid

1-Aminocyclohexane-1,3-dicarboxylic acid is a fascinating compound that plays a significant role in various fields of chemistry. Here are some noteworthy points about this compound:

  • Structure and Functionality: This compound features a cyclohexane ring with two carboxylic acid groups and one amino group, making it an important intermediate in organic synthesis.
  • Versatile Applications: It is utilized in the production of biodegradable polymers and biologically active molecules, enhancing its relevancy in industrial chemistry and pharmaceuticals.
  • Synthesis: One interesting aspect of this compound is its synthesis, which often involves multi-step reactions. Chemists are fascinated by the various methods that can be employed to construct this complex molecule.
  • Biological Relevance: The structure resembles certain amino acids, which highlights its potential biological activity and makes it a candidate for further research in biochemical applications.
  • Chiral Nature: As a chiral compound, the different enantiomers of 1-aminocyclohexane-1,3-dicarboxylic acid can exhibit unique properties, potentially leading to diverse applications in medicinal chemistry.
  • Research Potential: Ongoing studies are investigating its role in creating pharmaceuticals that can mimic natural biological processes, showcasing the compound’s importance in drug design.

In conclusion, 1-aminocyclohexane-1,3-dicarboxylic acid is not only an intriguing compound due to its structure but also due to its broad applications and potential in scientific research. As we continue to explore the possibilities of this compound, we may unlock new innovations in chemistry and medicine.

Synonyms
SCHEMBL2916853
1-amino-1,3-dicarboxycyclohexan