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Cyclic Amino Acid

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Identification
Molecular formula
C5H7NO4
CAS number
16856-18-1
IUPAC name
2-[amino(carboxy)methyl]cyclopropanecarboxylic acid
State
State

This compound exists as a solid at room temperature. It is often found in a white powder form due to its crystalline structure.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.00
Boiling point (Celsius)
306.00
Boiling point (Kelvin)
579.00
General information
Molecular weight
129.11g/mol
Molar mass
129.1270g/mol
Density
1.4600g/cm3
Appearence

The compound typically appears as a white crystalline solid. Its structure includes a cyclopropane ring, which contributes to its solid form and crystalline nature.

Comment on solubility

Solubility of 2-[amino(carboxy)methyl]cyclopropanecarboxylic acid

The solubility of 2-[amino(carboxy)methyl]cyclopropanecarboxylic acid (C5H7NO4), often referenced in discussions about amino acids and their derivatives, can be characterized by several key factors:

  • Polarity: The presence of multiple functional groups, including amino and carboxylic acid groups, contributes to a high level of polarity in this compound. This typically enhances its ability to dissolve in polar solvents, particularly water.
  • Hydrogen Bonding: The amino group (–NH2) and carboxylic acid groups (–COOH) allow the molecule to form strong hydrogen bonds with water molecules, further facilitating solubility.
  • pH Dependency: The solubility can be affected by the pH of the solution. At various pH levels, the ionization state of the carboxylic acid can change, which may either enhance or hinder solubility.

Due to these characteristics, 2-[amino(carboxy)methyl]cyclopropanecarboxylic acid is soluble in aqueous environments. In summary, it is a versatile compound that demonstrates substantial solubility in water because of its functional groups and ionic nature.

Interesting facts

Interesting Facts about 2-[amino(carboxy)methyl]cyclopropanecarboxylic acid

2-[amino(carboxy)methyl]cyclopropanecarboxylic acid, commonly known as ACMCA, is a fascinating compound in the realm of organic chemistry. This compound is noteworthy for several reasons:

  • Unique Structure: The cyclopropane ring in ACMCA introduces strain to the molecule, making it reactive and interesting for various chemical reactions. The combination of amino and carboxylic acid functional groups also grants it interesting properties for biochemical applications.
  • Biological Relevance: ACMCA is of particular interest in the field of amino acid research. Certain modifications of this compound can lead to the synthesis of amino acids that are essential for various biological processes.
  • Potential Applications: This compound can play a role in developing pharmaceuticals, as its structural characteristics might influence the efficacy and interactions of drug molecules.
  • Synthesis Challenges: The synthetic routes leading to ACMCA can be quite intricate due to the need to create both the cyclopropane structure and the appropriate functional groups, thus offering a great exercise in organic synthesis techniques.
  • Research Opportunities: Chemists are continually exploring ways to leverage the unique properties of ACMCA for applications in fields such as agrochemicals, making this compound a potential candidate for innovative research.

In summary, 2-[amino(carboxy)methyl]cyclopropanecarboxylic acid not only possesses a unique molecular architecture but also serves as a valuable compound for chemical investigations and potential applications in various scientific fields.

Synonyms
CCPG
22255-17-0
(alpha-Carboxycyclopropyl)glycine
2-[amino(carboxy)methyl]cyclopropane-1-carboxylic acid
3,4-Cyclopropylglutamate
L-2-(Carboxypropyl)glycine
L-trans-alpha-Amino-2-carboxycyclopropaneacetic acid
2-(amino(carboxy)methyl)cyclopropane-1-carboxylic acid
L-CCG III
L-CCG I
alpha-(Carboxycyclopropyl)glycine
2-(amino(carboxy)methyl)cyclopropanecarboxylic acid
2-[amino(carboxy)methyl]cyclopropanecarboxylic acid
Cyclopropaneacetic acid, alpha-amino-2-carboxy-
Cyclopropaneaceticacid, a-amino-2-carboxy-
alpha-Amino-2-carboxycyclopropaneacetic acid
SCHEMBL10379762
DTXSID20944912
CHEBI:173420
GZOVEPYOCJWRFC-UHFFFAOYSA-N
PDSP1_000810
PDSP2_000797
AKOS030592508
L000347
(1R,2S)-2-[(1S)-1-amino-2-hydroxy-2-oxo-ethyl]cyclopropanecarboxylic acid