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1-Aminocyclopentane-1,3-dicarboxylic Acid

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Identification
Molecular formula
C7H11NO4
CAS number
277779-06-1
IUPAC name
1-aminocyclopentane-1,3-dicarboxylic acid
State
State

At room temperature, 1-aminocyclopentanecarboxylic acid is in solid state, typically presenting as a stable, crystalline powder.

Melting point (Celsius)
201.00
Melting point (Kelvin)
474.15
Boiling point (Celsius)
351.10
Boiling point (Kelvin)
624.25
General information
Molecular weight
173.17g/mol
Molar mass
173.1750g/mol
Density
1.4600g/cm3
Appearence

1-Aminocyclopentane-1,3-dicarboxylic acid typically appears as a white to off-white crystalline powder. This solid form has a characteristic crystalline structure.

Comment on solubility

Solubility of 1-aminocyclopentane-1,3-dicarboxylic acid (C7H11NO4)

The solubility of 1-aminocyclopentane-1,3-dicarboxylic acid is an intriguing characteristic that is influenced by its polar functional groups and cyclic structure. This compound contains both carboxylic acid groups and an amine group, which generally enhances solubility in polar solvents. Here are some key points regarding its solubility:

  • Water Solubility: The presence of two carboxylic acid groups contributes to a higher likelihood of solubility in water due to hydrogen bonding capabilities.
  • Solvent Compatibility: It is expected to be more soluble in polar solvents (such as water and ethanol) than in non-polar solvents (like hexane).
  • Temperature Influence: Solubility can increase with temperature, allowing for greater dispersion in solutions, especially when considering biological environments.

When assessing solubility, it's important to consider not just the compound’s structure, but also the operational conditions. As a rule of thumb, compounds with a higher number of hydrogen-bonding groups tend to show better solubility characteristics. As always, empirical testing may provide the most reliable data on solubility behaviors in specific environments.

Interesting facts

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

1-Aminocyclopentane-1,3-dicarboxylic acid is a fascinating compound that possesses unique structural properties and applications in various scientific fields. Here are some intriguing insights about this compound:

  • Structure and Isomerism: The compound features a cyclopentane ring with functional groups that lead to interesting isomeric forms. The presence of both amino and carboxylic acid groups makes it a key player in amine chemistry and carboxylic acid reactivity.
  • Biological Relevance: This compound is notable for its role in biological systems. It can act as an intermediate in the biosynthesis of certain amino acids and plays a role in various metabolic pathways.
  • Potential Applications: 1-Aminocyclopentane-1,3-dicarboxylic acid has potential applications in the pharmaceutical industry. Its unique structure may allow it to serve as a building block for the synthesis of novel drugs and biologically active compounds.
  • Research Opportunities: Chemists are exploring the compound for its potential use in asymmetric synthesis and as a chiral auxiliary. The presence of both the amine and carboxyl groups may allow for interesting reactivity and selectivity in synthetic processes.
  • Synthesis Techniques: The synthesis of 1-aminocyclopentane-1,3-dicarboxylic acid can involve various methods, including decarboxylative coupling and other innovative synthetic strategies, making it a subject of interest for organic chemists.

With its intriguing properties and multifaceted applications, 1-aminocyclopentane-1,3-dicarboxylic acid stands as a testament to the diversity and complexity of organic compounds. As research continues, it may reveal even more exciting potential in various scientific realms!

Synonyms
1-aminocyclopentane-1,3-dicarboxylic acid
100910-67-6
1-Amino-1,3-cyclopentanedicarboxylic acid
ACPD
1,3-Cyclopentanedicarboxylicacid, 1-amino-, (1R,3R)-
67684-64-4
39026-63-6
(+/-)-1-AMINOCYCLOPENTANE-cis-1,3-DICARBOXYLIC ACID
1S, 3R-ACPD
SCHEMBL235442
BDBM86212
DTXSID701272273
HMS3266A17
477331-06-9
CUA33106
CAS_104766
NSC_104766
LS-13300
DB-017863
DB-126829
L001124
Q4650770