Skip to main content

Furancarboxyglycine

ADVERTISEMENT
Identification
Molecular formula
C7H7NO4
CAS number
959-46-4
IUPAC name
2-(furan-2-carbonylamino)acetic acid
State
State

At room temperature, Furancarboxyglycine is typically in a solid state. This is due to its molecular structure that allows it to form stable crystalline lattices. In solid form, it is relatively stable but should be stored properly to maintain its integrity.

Melting point (Celsius)
155.00
Melting point (Kelvin)
428.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
155.14g/mol
Molar mass
155.1270g/mol
Density
1.5025g/cm3
Appearence

In its pure form, Furancarboxyglycine appears as a solid crystalline powder. The color can range from white to light beige, depending on the specific sample and its purity. It is important to handle this compound under appropriate conditions to ensure its stability and to prevent degradation.

Comment on solubility

Solubility of 2-(furan-2-carbonylamino)acetic acid

2-(furan-2-carbonylamino)acetic acid is a compound characterized by its unique structural features, which influence its solubility properties. The solubility of this compound can be understood through several factors:

  • Polarity: The presence of the amino acid group enhances polarity, which often leads to improved solubility in polar solvents such as water.
  • Functional Groups: The carbonyl and amino groups present in the molecule are known for forming hydrogen bonds, increasing the compound's ability to interact with solvent molecules.
  • pH Influence: The solubility of 2-(furan-2-carbonylamino)acetic acid may vary with pH; at certain pH levels, the formation of ionic species can further enhance solubility.

In general terms, one can expect that:

  • It is likely to be more soluble in aqueous solutions relative to non-polar solvents.
  • Increased temperature may also enhance solubility, a common behavior observed in many similar compounds.

Overall, while specific empirical data would provide more definitive insights, the combination of functional groups in 2-(furan-2-carbonylamino)acetic acid suggests a strong likelihood of moderate to high solubility in polar solvents.

Interesting facts

Interesting Facts about 2-(furan-2-carbonylamino)acetic acid

2-(furan-2-carbonylamino)acetic acid is a fascinating compound that combines both a furan moiety and an amino acid structure. Here are some intriguing aspects of this compound:

  • Biological Relevance: This compound has potential applications in pharmacology and biochemistry due to its structural similarity to natural amino acids, which makes it a valuable candidate for studying enzyme interactions and metabolic pathways.
  • Cyclic Structure: The presence of the furan ring contributes to the compound's reactivity and stability, allowing it to engage in complex biochemical processes.
  • Amide Bond: The carbonylamine functional group in the compound plays a crucial role in forming amide bonds, which are essential in peptide synthesis and protein structure.

This compound is part of a broader class of molecules known as heterocycles, which are aromatic compounds containing at least one atom that is not carbon. The furan ring is an example of a five-membered heterocycle, and it has been a topic of interest because of its naturally occurring derivatives found in various plant species.

Researchers are particularly interested in the potential of 2-(furan-2-carbonylamino)acetic acid in drug design, where modifications to the furan ring can lead to novel therapeutic agents. As synthesized compounds derived from natural products often possess unique biological narratives, they frequently serve as a basis for pharmaceutical innovation.

In summary, 2-(furan-2-carbonylamino)acetic acid serves not only as an intriguing subject for the study of organic synthesis but also reflects the interconnectedness of chemistry and biology in the quest for new materials and medical treatments.

Synonyms
N-(2-Furoyl)glycine
5657-19-2
Furoylglycine
2-Furoylglycine
2-(furan-2-carbonylamino)acetic acid
Pyromucurate
(2-Furoylamino)acetic acid
BRN 0142378
N-2-furoyl-Glycine
CHEBI:82912
N-(furan-2-ylcarbonyl)glycine
DTXSID50205124
4-18-00-03955 (Beilstein Handbook Reference)
N-(carboxymethyl)-2-Furancarboxamide
[[(Furan-2-yl)carbonyl]amino]acetate
(((Furan-2-yl)carbonyl)amino)acetate
DTXCID50127615
kspqdmrtzzyqlm-uhfffaoysa-n
Pyromucuric acid
Furfuroylglycine
N-(2-Furanylcarbonyl)glycine
Furoilglicina
Furoilglicina [Italian]
Glycine, N-(2-furanylcarbonyl)-
2-(Furan-2-carboxamido)acetic acid
GLYCINE, N-2-FUROYL-
2-(2-Furoylamino)acetic acid
(((Furan-2-yl)carbonyl)amino)acetic acid
[[(Furan-2-yl)carbonyl]amino]acetic acid
2-FUROYL GLYCINE
N-2-furoylglycine
Glycine, 1-furoyl-
Enamine_005285
bmse000615
SCHEMBL237337
[(2-furoyl)amino]acetic acid
N-(2-Furoyl)glycine, 98%
CHEMBL456404
HMS1409A05
2-(furan-2-ylformamido)acetic acid
MFCD00030606
AKOS000264526
2-[(furan-2-yl)formamido]acetic acid
[(furan-2-carbonyl)-amino]-acetic acid
BS-42199
FF179430
Glycine, N-(2-furanylcarbonyl)- (9CI)
PD167027
DB-052940
HY-113340
CS-0059646
EU-0032785
NS00015704
EN300-08091
G12084
AG-205/06486029
Q27156454