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N-Acetylanthranilic acid

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Identification
Molecular formula
C15H13NO3
CAS number
89-52-1
IUPAC name
2-(2-amino-3-benzoyl-phenyl)acetic acid
State
State

At room temperature, N-Acetylanthranilic acid exists as a solid in the form of crystalline powder.

Melting point (Celsius)
182.00
Melting point (Kelvin)
455.15
Boiling point (Celsius)
391.70
Boiling point (Kelvin)
664.85
General information
Molecular weight
241.26g/mol
Molar mass
241.2630g/mol
Density
1.3843g/cm3
Appearence

N-Acetylanthranilic acid appears as a white to off-white crystalline powder. Its solid form is typically housed in a stable structure of fine crystals.

Comment on solubility

Solubility of 2-(2-amino-3-benzoyl-phenyl)acetic acid

The solubility of 2-(2-amino-3-benzoyl-phenyl)acetic acid (C15H13NO3) can be characterized by several distinctive features:

  • Polar and Non-Polar Interaction: The presence of both an amino group and a carboxylic acid functional group allows this molecule to engage in polar interactions, while the benzoyl and phenyl rings introduce non-polar character.
  • Solvent Dependence: This compound is expected to demonstrate varying solubility in different solvents. Generally, it is more soluble in polar solvents like methanol and ethanol due to hydrogen bonding capabilities.
  • pH Influence: The solubility can also be affected by the pH of the solution. In acidic conditions, the carboxylic acid group may remain protonated, while in more basic conditions, it can deprotonate, increasing solubility.

Overall, the solubility of 2-(2-amino-3-benzoyl-phenyl)acetic acid is influenced by its functional groups, the solvent used, and the pH of the environment, making it an interesting compound for studies related to solubility behavior.

Interesting facts

Interesting Facts about 2-(2-amino-3-benzoyl-phenyl)acetic acid

2-(2-amino-3-benzoyl-phenyl)acetic acid, often referred to as a complex organic compound, showcases a unique structure that offers both medicinal and synthetic chemistry applications. Here are some intriguing highlights about this compound:

  • Structural Complexity: This compound features a benzoyl group and an amino group, contributing to its reactivity and the potential for forming various derivatives.
  • Biological Significance: Compounds with similar structures are known for their role as pharmaceutical intermediates, potentially influencing neurochemical pathways.
  • Research Interest: Scientists are particularly interested in the compound's properties for developing new drugs targeting specific receptors due to its unique functional groups.
  • Synthesis Potential: The synthesis of 2-(2-amino-3-benzoyl-phenyl)acetic acid often involves multi-step reactions, showcasing the importance of advanced organic techniques in the laboratory.
  • Chiral Molecule: Being a chiral molecule, it may exist in different enantiomeric forms, which could affect its biological activity and interactions in vivo.

As quoted in scientific literature, *“The myriad applications of such complex frameworks in pharmaceuticals cannot be overstated.”* This compound serves as a prime example of the exciting intersection of organic chemistry and medicinal development. Its exploration continues to open new avenues for research and innovation in the field.

Synonyms
Amfenac
51579-82-9
Amfenaco
2-(2-amino-3-benzoylphenyl)acetic acid
Amfenacum
(2-Amino-3-benzoylphenyl)acetic acid
(2-Amino-3-benzoylphenyl)essigsaeure
Amfenac [INN:BAN]
Amfenacum [INN-Latin]
CHEBI:75915
Amfenaco [INN-Spanish]
Fenazox (Japan)
Amfenac (INN)
amfenac sodium
NSC-309467
UNII-28O5C1J38A
28O5C1J38A
AMFENAC [INN]
AMFENAC [MI]
2-amino-3-benzoylbenzeneacetic acid
AMFENAC [WHO-DD]
NSC 309467
DTXSID90199533
AHR-5850D
Amfenacum (INN-Latin)
2-[2-amino-3-(benzoyl)phenyl]acetic acid
Amfenaco (INN-Spanish)
Amfenac sodium anhydrous
Amfenac sodium salt hydrate
2-(2-amino-3-(benzoyl)phenyl)acetic acid
2-Amino-3-Benzoylphenylacetic Acid
SCHEMBL24249
CHEMBL25146
GTPL7565
DTXCID50122024
SOYCMDCMZDHQFP-UHFFFAOYSA-N
BDBM50225110
MFCD00866133
NSC309467
AKOS022183018
2-(2-amino-3-benzoylphenyl)aceticacid
SY265113
DB-082510
NS00040651
D07443
SR-01000944946
Q4745976
SR-01000944946-1
BRD-K82122102-323-01-1