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Oxalyl glycine

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Identification
Molecular formula
C11H10N2O4
CAS number
83991-06-0
IUPAC name
2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid
State
State

Oxalyl glycine is in a solid state at room temperature. It is often handled as a crystalline powder for research applications.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
245.00
Boiling point (Kelvin)
518.15
General information
Molecular weight
224.21g/mol
Molar mass
224.2090g/mol
Density
1.3950g/cm3
Appearence

Oxalyl glycine is typically a white crystalline solid. Its appearance may vary depending on the purity and form (e.g., powder or crystalline).

Comment on solubility

Solubility of 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid (C11H10N2O4)

The solubility of 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid is an interesting topic due to its complex structure and functional groups. This compound exhibits properties that can influence its interaction with solvents. Generally, the solubility can be described considering several factors:

  • Polarity: The presence of amino (-NH2) and carboxylic acid (-COOH) groups makes the molecule polar, enhancing its solubility in polar solvents like water.
  • Hydrogen Bonding: The ability of 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid to form hydrogen bonds with water molecules increases its solubility, enabling it to dissolve effectively in aqueous environments.
  • pKa Values: The pKa values of the acidic functional groups in the compound will determine the ionization state in different pH environments, which in turn will affect its solubility. In an ideal pH range, the acid can be more soluble.
  • Compatibility with Other Solvents: While it is soluble in water, it may also exhibit varying solubility in organic solvents, depending on their polarity. For example, alcohols or dimethyl sulfoxide (DMSO) can also serve as good solvents.

In summary, the solubility characteristics of 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid reveal its potential in various applications. It would likely be more soluble in polar solvents due to its functional groups and could play a role in drug formulation or biochemical studies.

Interesting facts

Discovering 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid

2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid is a fascinating chemical compound that showcases the complexity and beauty of organic chemistry. This compound belongs to a class of molecules that often exhibit interesting biological activities, making them subjects of extensive research and potential therapeutic exploration.

Key Features

  • Diverse Applications: Compounds like this one have potential implications in pharmaceuticals, particularly in the design of drugs targeting various diseases.
  • Functionality: The presence of an amino group and a formamide moiety contributes to the compound’s ability to participate in hydrogen bonding and other intermolecular interactions. This can influence its chemical reactivity and biological efficacy.
  • Research Interest: Chemical compounds that include both an amine and a carbonyl group often present unique reactivity patterns, making them of great interest in synthetic organic chemistry.

Researchers are excited about compounds such as 2-amino-4-(2-formamidophenyl)-4-oxo-butanoic acid due to their potential to serve as intermediates in synthesis or as scaffold molecules in drug design. The structured framework provided by this compound may facilitate the development of new therapeutic agents aimed at addressing critical health challenges. Indeed, the ongoing studies involving this compound contribute greatly to our understanding of how molecular structure influences biological activity.

As quoted by a prominent chemist, "Chemistry is the art of transformation, and every compound tells a story of potential." This compound exemplifies that sentiment, representing not just its molecular makeup but also the myriad possibilities it encompasses in the realms of science and medicine.

Synonyms
N-formylkynurenine
1022-31-7
N'-formylkynurenine
2-amino-4-(2-formamidophenyl)-4-oxobutanoic acid
Formylkynurenine
Benzenebutanoic acid, alpha-amino-2-(formylamino)-gamma-oxo-
N3FFD7AJC9
3-(n-formylanthraniloyl)-alanine
NSC-334199
N'-formyl-Kynurenine
N-formyl-delta-kynurenine
UNII-N3FFD7AJC9
SCHEMBL148492
3-(2-formamidobenzoyl)alanine
MEGxm0_000151
FORMYLKYNURENINE, (DL)-
CHEBI:18377
DTXSID10862515
FORMYLKYNURENINE, (+/-)-
Alanine, 3-(N-formylanthraniloyl)-
NSC334199
AKOS022659639
N'-FORMYLKYNURENINE, (+/-)-
AS-85056
N inverted exclamation marka-Formylkynurenine
NS00120577
G72422
Q71982
Alanine, 3-(N-formylanthraniloyl)- (6CI,7CI,8CI)
ALANINE, 3-(N-FORMYLANTHRANILOYL)-, (+/-)-
alpha-amino-2-(formylamino)-gamma-oxo-Benzenebutanoate
alpha-amino-2-(formylamino)-gamma-oxo-Benzenebutanoic acid
Benzenebutanoic acid, alpha-amino-2-(formylamino)-gamma-oxo- (9CI)
N'-Formylkynurenine is known as a photooxidation product of Tryptophan.
BENZENEBUTANOIC ACID, .ALPHA.-AMINO-2-(FORMYLAMINO)-.GAMMA.-OXO-, (+/-)-